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UNIVERSIDADE FEDERAL DE PERNAMBUCO
CENTRO DE CIÊNCIAS BIOLÓGICAS
PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS BIOLÓGICAS
KÁTIA KELLE DA SILVA ANDRADE ALBUQUERQUE
EXTRAÇÃO EM SISTEMA DE DUAS FASES AQUOSAS (PEG/CITRATO),
CARACTERIZAÇÃO E APLICAÇÃO DA TANASE DE Aspergillus sp. SIS 25 EM
CHÁ VERDE (Camellia sinensis)
RECIFE
2016
UNIVERSIDADE FEDERAL DE PERNAMBUCO
CENTRO DE CIÊNCIAS BIOLÓGICAS
PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS BIOLÓGICAS
EXTRAÇÃO EM SISTEMA DE DUAS FASES AQUOSAS (PEG/CITRATO),
CARACTERIZAÇÃO E APLICAÇÃO DA TANASE DE Aspergillus sp. SIS 25 EM
CHÁ VERDE (Camellia sinensis)
KÁTIA KELLE DA SILVA ANDRADE
ALBUQUERQUE.
Dissertação apresentada ao Programa de
Pós-Graduação em Ciências Biológicas da
Universidade Federal de Pernambuco,
como parte dos requisitos para obtenção
do título de Mestre em Ciências
Biológicas.
Área de Concentração: Biotecnologia.
Orientadora: Prof.ª Dr.ª Ana Lúcia
Figueiredo Porto.
Co-Orientadora: Dr.ª Polyanna Nunes
Herculano.
RECIFE
2016
Catalogação na Fonte:
Bibliotecário Bruno Márcio Gouveia, CRB-4/1788
Albuquerque, Kátia Kelle da Silva Andrade
Extração em sistema de duas fases aquosas (PEG/Citrato) caracterização e
aplicação da tanase de Aspergillus sp. SIS 25 em chá verde (Camellia sinensis / Kátia
Kelle da Silva Andrade Albuquerque. – Recife: O Autor, 2016.
67 f.: il.
Orientadores: Ana Lúcia Figueiredo Porto, Polyanna Nunes Herculano
Dissertação (mestrado) – Universidade Federal de Pernambuco. Centro
de Ciências Biológicas. Programa de Pós-graduação em Ciências
Biológicas, 2016.
Inclui referências
1. Enzimas 2. Fungos – Enzimas I. Porto, Ana Lúcia Figueiredo (orient.) II.
Herculano, Polyanna Nunes (coorient.) III. Título.
572.7 CDD (22.ed.) UFPE/CCB-2016-148
KÁTIA KELLE DA SILVA ANDRADE ALBUQUERQUE
Dissertação apresentada ao Programa de Pós-
Graduação em Ciências Biológicas da
Universidade Federal de Pernambuco, como
parte dos requisitos para obtenção do título de
Mestre em Ciências Biológicas.
Área de Concentração: Biotecnologia.
Data da aprovação: 19 de fevereiro de 2016.
COMISSÃO EXAMINADORA
MEMBROS TITULARES
__________________________________________
Prof.ª Dr.ª Ana Lúcia Figueiredo Porto
(Universidade Federal de Pernambuco)
__________________________________________
Dr.ª Cynthia de Oliveira Nascimento
(Universidade Federal Rural de Pernambuco)
_________________________________________
Dr. Romero Marcos Pedrosa Brandão Costa
(Universidade Federal Rural de Pernambuco)
A fé é o firme fundamento das coisas que se esperam, e
a prova das coisas que não se vêem.
Hebreus 11:1
AGRADECIMENTOS
“Até aqui nos ajudou o Senhor”. I Samuel 7:12
Agradeço a Deus pela companhia diária, pois foi por Sua infinita bondade e
misericórdia que cheguei até aqui.
Agradeço à minha família, especialmente à minha mãe Lucivânia, meu esposo
Salomão Jr. e minha sogra Usiene, pelo apoio constante e por toda compreensão e
preocupação. Às minhas lindas “bonecas” Júlia e Laura que enchem a minha casa de alegria e
me ensinam a leveza de ser como criança. Sou imensamente grata às minhas amigas-irmãs
pelas inúmeras palavras de ânimo, pelas orações e por toda ajuda dedicada a esta dissertação.
Vocês são um presente de Deus para mim!
Agradeço às professoras Ana Porto e Polyanna Herculano pela orientação e acolhida
no LABTECBIO. Meus sinceros agradecimentos aos PNPD’s do laboratório e aos amigos de
bancada que ao longo desses 4 anos de convivência no laboratório dividiram comigo sorrisos,
alegrias, frustrações, os cadernos de protocolos, conhecimentos de inglês, matemática e de
Excel. Sem dúvidas o apoio de vocês foi fundamental para que eu concluísse esse trabalho.
Aos novos amigos que vieram com o mestrado: obrigada pelo companheirismo e pela
amizade que ficou depois que das disciplinas.
Por fim, agradeço à UFPE e ao PPGCB pela minha formação e à CAPES pelo
incentivo financeiro.
RESUMO
Enzimas são proteínas com atividade catalítica capazes de integrar diferentes processos
biotecnológicos. Dentre as enzimas com aplicação na indústria destaca-se a tanino acil
hidrolase (EC 3.1.1.20) ou simplesmente tanase, uma enzima extracelular produzida na
presença de ácido tânico por fungos filamentosos, bactérias e leveduras. A tanase (TAH)
catalisa a hidrólise de taninos liberando ácido gálico e glicose. TAH pode ser utilizada no
tratamento de efluentes, na indústria farmacêutica, de alimentos, bebidas entre outros. Na
biotecnologia, o grande desafio na produção de enzimas é extrair a molécula a partir de
métodos economicamente viáveis. Assim, o sistema de duas fases aquosas (SDFA) tem sido
cada vez mais utilizado para purificar parcialmente diversos produtos biológicos. Neste
sentido, o presente trabalho teve como finalidade extrair em SDFA, caracterizar
bioquimicamente e aplicar em chá verde a enzima tanase obtida de Aspergillus sp. SIS 25 por
fermentação em estado sólido, utilizando a fibra do coco como substrato. Um planejamento
fatorial 23 foi utilizado para avaliar a influência das variáveis principais: massa molar
(MMPEG) do PEG (1000, 3350 e 6000 g/mol), concentração (20, 22 e 24% m/m) do PEG
(CPEG) e concentração (15, 17,5 e 20% m/m) de citrato de sódio (CCIT), sobre as variáveis
resposta: coeficiente de partição (K), recuperação (Rec) e aumento de pureza (AP), em pH 6.
A tanase foi preferencialmente particionada para a fase sal do sistema uma vez que em todos
os ensaios os valores de K foram menores do que 1. As variáveis MMPEG e a interação entre
MMPEG-CPEG apresentaram os resultados mais significativos para o valor de K, sendo ambos
os efeitos negativos. Com relação ao aumento de pureza, o melhor resultado (3,2) foi
observado no ensaio 8 com 24% de PEG 6000 e 20% de sal. A tanase extraída do sistema
apresentou temperatura ótima a 30° C e pH ótimo 5,0. A perda da estabilidade foi observada a
50 °C. A TAH desse estudo foi estimulada na presença de Na+ e completamente inibida na
presença de Zn2+
. Os surfactantes não interferiram significativamente em sua atividade, com
exceção do Triton X-100 a 2% que diminuiu a atividade relativa em aproximadamente 50%.
No processo de hidrólise dos compostos fenólicos do chá verde, a tanase pré-purificada em
SDFA apresentou melhor resultado se comparada ao extrato bruto; 0,75 mL da enzima do
sistema reduziu 44% dos fenóis do chá. Os resultados demonstram que o modelo estatístico
montado para o SDFA além de permitir a extração de uma tanase parcialmente pura tornou
conhecido outros modelos que favorecem a otimização das variáveis estudadas,
principalmente o aumento de pureza. Com isso, é possível afirmar que a tanase de Aspergillus
sp. SIS 25 pode ser extraída através de um método de baixo custo, que emprega material
reutilizável, biodegradável e que o processo conservou as características biquímicas dessa
enzima devido à abundância de água que ocorre no sistema e pela utilização de componentes
inertes à maioria das bimoléculas. A criação desse ambiente favorável para separar moléculas
biológicas pode explicar o fato da tanase não ter perdido sua atividade durante o estudo,
mantendo sua ação catalítica principalmente durante a aplicação em chá verde.
Palavras-chave: sistema de duas fases aquosas, Aspergillus sp., purificação, tanase, chá
verde.
ABSTRACT
Enzymes are proteins with catalytic activity capable of integrating different biotechnological
processes. One of the enzymes with application in industry stands out the tannin acyl
hydrolase (EC 3.1.1.20) or simply tannase, an extracellular enzyme produced in the presence
of tannic acid by filamentous fungi, bacteria and yeast. The tannase (TAH) catalyzes the
hydrolysis of tannins releasing gallic acid and glucose. TAH can be used for effluent
treatment, pharmaceutical industry, food, beveragesand others. In biotechnology, the big
challenge in the production of enzymes is to extract the molecule from economically viable
methods. Thus, the aqueous two-phase system (ATPS) has been increasingly used to
partiallypurify biological products. In this sense, the present work had as purpose to extract in
ATPS, characterize biochemically and apply in green tea the tannase enzyme obtained from
Aspergillus sp. SIS 25 by solid state fermentation using coconut fiber like substrate. A
factorial design 23 was used to evaluate the influence of major variables: PEG molar mass
(1000, 3350 and 6000 g/mol), PEG concentration (CPEG) and sodium citrate concentration
(CCIT), on the response variables: partition coefficient (K), recovery (Rec) and purity
increase (AP), at pH 6. The tanase was preferentially partitioned to stage the salt system once
in all tests the values of K were lower than 1. The variables MMPEG and the interaction
between MMPEG-CPEG presented the results more meaningful for the value of K, being both
negative effects. With regard to the increase in purity, the best result (3.2) was observed in 8
test with 24% of PEG 6000 and 20% salt. The tannase extracted from system showed
optimum temperature at 30 ° C and optimum pH 5.0. The loss of stability was observed at 50°
c. TAH this study was stimulated in the presence of Na+ and completely inhibited in the
presence of Zn2+
. Surfactants not significantly interfere in their activity, with the exception of
Triton X-100 2% that decreased the relative activity by approximately 50%. In the process of
hydrolysis of phenolic compounds from green tea, tannase pre-purified in ATPS showed
better results when compared to the crude extract; 0.75 ml of the enzyme from system has
reduced 44% of tea phenols. The results show that the statistical model fitted to the ATPS and
allow the extraction of a pure and partially known other models that favor the optimization of
the studied variables, especially the increase in purity. With this, it is possible to affirm that
the tanase of Aspergillus sp. SIS 25 can be extracted through a low-cost method, employing
reusable, biodegradable material and the process preserved the biquímicas features of this
enzyme because of the abundance of water that occurs in the system and by the use of inert
components to most bimoléculas. The creation of this favourable environment to separate
biological molecules can explain the fact of tannase didn't lose its activity during the study,
keeping their catalytic action primarily during application in green tea.
Keywords: aqueous two-phase systems, Aspergillus, purification, tannase, green tea.
LISTA DE FIGURAS
Pág.
CAPÍTULO 1
REVISÃO DA LITERATURA
Figura 1. Estrutura molecular de um galotanino. 04
Figura 2. Reação de hidrólise do ácido tânico, R1 (galoil) e R2 (digaloil) pela
tanase.
05
CAPÍTULO 2
Extraction in aqueous two-phase system (PEG/Citrate), characterization and
application of tannase from Aspergillus sp. SIS 25 in green tea (Camellia sinensis)
Figure 1. Pareto chart of the main effects and their interactions for the response
variable K in the tanase extraction process in ATPS PEG/citrate using full statistical
planning 23.
26
Figure 2. Pareto chart of the main effects and interactions for variable Yeld (%) in
the tanase extraction process in ATPS PEG / citrate using full statistical design 23,
in bottom phase.
27
Figure 3. Influence of different temperatures in the activity of tannase produced by
Aspergillus sp. 25 SIS (A) and enzyme stability for 3 hours of incubation (B).
28
Figure 4. Influence of different pH in the activity of tannase produced by
Aspergillus sp. SIS 25 after 30 minutes of incubation.
29
Figure 5. Influence of various metal ions concentration on tannase activity of
Aspergillus sp. SIS 25, extracted in aqueous two-phase system.
31
Figure 6. Pigment retention in the PEG phase (top) of the ATPS (A) and qualitative
difference in color of green tea (1), green tea treated with partially purified tannase
(2) and green tea with crude extract (B).
32
LISTA DE TABELAS
Pág.
CAPÍTULO 2
Extraction in aqueous two-phase system (PEG/Citrate), characterization and
application of tannase from Aspergillus sp. SIS 25 in green tea (Camellia sinensis)
Table 1. Variable levels of the 23 experimental design selected for tannase
extraction by PEG/citrate ATPS
22
Table 2. Combinations of the levels of three independent variables (concentration
of PEG and sodium citrate and molecular weight of PEG) used in a complete
factorial design 23 and the values of the relative responses
25
Table 3. Influence of various surfactants on tannase enzyme activity. 30
Table 4. Effect of concentration of 0.75 mL of crude extract and 0.75 mL of
purified tannase enzyme in ATPS (PEG /Citrate) on hidrolyzes of 1mL green tea
phenolic compounds.
33
LISTA DE ABREVIATURAS E SIGLAS
PEG Polietileno glicol
K Coeficiente de partição
SDFA Sistema de duas fases aquosas
TAH Tanino acil hidrolase
MMPEG Massa Molar do Polietileno glicol
CPEG Concentração de Polietileno glicol
CCIT Concentração de citrato
Rec Recuperação
ATPS Aqueous two phase systems
Da Daltons
kDa Quilodaltons
ANOVA Análise de Variância
pH Potencial hidrogênionico
RPM Rotações por minuto
SDS Dodecil sulfato de sódio
B.O.D. Biochemical oxygen demand
BCA Ácido bicinconínico
AP Aumento de pureza
PAGE Gel de poliacrilamida
SUMÁRIO
Pág.
RESUMO
ABSTRACT
LISTA DE FIGURAS
LISTA DE TABELAS
LISTA DE ABREVIATURAS E SIGLAS
INTRODUÇÃO 02
CAPÍTULO 1 04
1. REVISÃO BIBLIOGRÁFICA 04
1.1 Taninos 04
1.2 Tanase 05
1.3 Fontes de obtenção da tanase 06
1.4 Gênero Aspergillus 07
1.5 Sistema de duas fases aquosas 08
1.6 Aplicações da tanase 09
1.7 Chá verde (Camellia sinensis) 10
2. REFERÊNCIAS BIBLIORÁFICAS 12
CAPÍTULO 2
Extraction in aqueous two-phase system (PEG/Citrate), characterization and
application of tannase from Aspergillus sp. SIS 25 in green tea (Camellia sinensis)
17
Abstract 18
1. INTRODUCTION 19
2. MATERIAL AND METHODS 21
2.1 Microorganisms 21
2.2 Solid state fermentation and crude extract 21
2.3 Protein determination 21
2.4 Tannase activity 21
2.5 Preparation of aqueous two-phase systems 22
2.5.1 Experimental design and statistical analysis 22
2.5.2 Partition coefficient 22
2.5.3 Activity yield 23
2.5.4 Purification factor 23
2.6 Enzymatic characterization 23
2.6.1 Effect and stability to temperature and pH influence on tannase activity 23
2.6.2 Effect of metal ions on tannase activity 23
2.6.3 Surfactant influence on the activity of tannase 24
2.7 Hydrolysis of undesirable phenolic compounds in green tea by the action of the
enzyme tannase
24
3. RESULTS AND DISCUSSION 25
3.1 Tannase extraction in aqueous two-phase system 25
3.2 Effect of temperature and pH on tannase activity 28
3.3 Influence of surfactants on enzyme activity 30
3.4 Effect of metal ions on the enzyme activity 31
3.5 Hydrolysis of undesirable phenolic compounds in green tea by the action of the
enzyme tannase
32
4. REFERENCES 35
CONSIDERAÇÕES FINAIS 38
ANEXO I – NORMAS DA RESVISTA 39
2
INTRODUÇÃO
Os taninos são os compostos mais abundantemente extraídos da biomassa vegetal,
depois da celulose, hemicelulose e lignina. Podem ser encontrados nas folhas, frutos, raízes e
sementes dos vegetais superiores. Devido ao sabor adstringente, os taninos atuam como um
mecanismo de defesa das plantas contra o ataque de herbívoros (ARBENZ; AVEROUS,
2015). Estes compostos possuem a propriedade de formar complexos insolúveis em água e
por isso são considerados fatores antinutricionais em alimentos, pois podem associar-se a
proteínas dificultando a digestão. Os taninos podem ser hidrolisados por ácidos, bases e
tanases de diferentes fontes microbianas (JIMÉNEZ et al., 2014; SILVA et al., 2010).
A tanase (tanino acil hidrolase - EC 3.1.1.20), é uma enzima extracelular e induzível,
que catalisa a hidrólise de taninos produzindo ácido gálico e glicose (MADEIRA-JUNIOR et
al., 2015). Tanino acil hidrolase (TAH) pode ser produzida por fungos filamentosos, bactérias,
leveduras e, por ser uma enzima de grande interesse comercial, sua aplicação está sendo
estudada principalmente na indústria farmacêutica, tratamento de efluentes do couro,
alimentos e bebidas como os chás instantâneos (JANA et al., 2014).
O chá é uma bebida muito apreciada em todo o mundo. O chá verde (Camellia
sinensis), em especial, é vastamente consumido em vários países, inclusive o Brasil, por
apresentar efeitos benéficos à saúde, como por exemplo: auxílio na prevenção do câncer e
doenças cardiovasculares, combate ao excesso de gordura no corpo, efeito antioxidante de
radicais livres, quelantes de metais, inibidores da lipoperoxidação, entre outros (SANTOS et
al., 2014; ZHANG et al., 2016). Na indústria de chás, a tanase ajuda a reduzir a formação de
precipitados na bebida, além de melhorar a coloração e sabor (CHÁVEZ-GONZÁLEZ et al.,
2012). Apesar de melhorar os aspectos sensoriais do chá, a aplicação de tanase na produção
de bebidas ainda é limitado devido aos custos para obtenção da enzima, principalmente no
que se refere à purificação, que é um processo bastante complexo.
Atualmente, o grande desafio da biotecnologia consiste em aplicar a enzima em
diferentes setores da indústria sem que para isso necessite recorrer a métodos de custos
elevados. Apesar dos micro-organismos serem fontes inesgotáveis de diversas enzimas, o
processo de extração de moléculas de interesse se torna dispendioso em virtude dos processos
empregados para separar a molécula alvo de moléculas contaminantes. Os métodos
3
convencionais para purificar biomoléculas geralmente incluem etapas muito complexas. Uma
alternativa viável é extrair a molécula de interesse em sistema bifásico aquoso (LIMA et al.,
2013).
Os sistemas de duas fases aquosas (SDFA) são formados pela incompatibilidade de
dois polímeros hidrofílicos ou um polímero e um sal. Por apresentar alto teor de água em
ambas as fases esses sistemas constituem um meio adequado para extração de biomoléculas,
pois preservam a estabilidade molecular das mesmas (ALI et al., 2014). Os componentes do
sistema quando se separam favorecem o particionamento do produto biológico para uma das
fases e, através de ensaios laboratoriais e estatísticos, é possível definir os parâmetros que
levam a uma separação ideal. Com isso, a simplicidade da técnica faz do SDFA um processo
atrativo e de fácil reprodução em larga escala para extrair enzimas de interesse comercial
(TANG et al., 2014).
Deste modo, o objetivo do presente trabalho é extrair em SDFA e caracterizar
bioquimicamente a tanase de Aspergillus sp. SIS 25, apresentando uma potencial aplicação
desta enzima na redução de compostos fenólicos indesejáveis do chá verde, promovendo a
purificação da biomolécula por um método baixo custo.
4
CAPÍTULO 1
1. REVISÃO DA LITERATURA
1.1 Taninos
Os compostos polifenólicos compreendem uma ampla gama de substâncias que
possuem pelo menos um grupo hidroxila (-OH) em um ou mais anéis fenólicos. A maioria dos
compostos fenólicos não são encontrados no estado livre na natureza, mas na forma de ésteres
ou heterosídeos sendo, portanto, solúveis em água e em solventes orgânicos polares
(CARVALHO et al., 2007; CARVALHO et al., 2012). Dentre estes encontram-se os taninos,
um subgrupo de compostos fenólicos possivelmente de maior tamanho. O termo tanino foi
originalmente utilizado para descrever certas substâncias orgânicas que serviam para curtir
peles de animais em um processo conhecido como tanning. Atualmente, este termo tem sido
amplamente aceito para classificar um grupo bastante heterogêneo de compostos fenólicos de
massa molecular relativamente alta (500-20000 Da) e de complexidade elevada - 12-16
hidroxilas em 5-7 anéis aromáticos por cada 1000 Da (OLIVAS-AGUIRRE et al., 2015).
Os taninos são o segundo maior grupo de fenóis abundantes na natureza. São
considerados produtos do metabolismo secundário das plantas e, geralmente podem ser
encontrados em maior quantidade nas cascas, raízes, folhas e frutos (LENIN; LOKESWARI;
SRI, 2015). Em função da sua estrutura química os taninos são classificados em dois grupos:
taninos hidrolisáveis (galotaninos e elagitaninos) e taninos condensados (proantocianidinas).
Os galotaninos em especial, são formados por várias moléculas de ácidos orgânicos
esterificados parcial ou totalmente a uma molécula de glucose. Esta associação é facilmente
hidrolisada em meio ácido, alcalino, através da água quente ou por meio de ação enzimática
(JANA et al., 2014).
Figura 1. Estrutura molecular de um galotanino (BHAT; SINGH; SHARMA, 1998).
Núcleo central
Ácido gálico
5
Taninos são capazes de formar ligações estáveis com proteínas e outros polímeros, tais
como os polissacarídeos. Por serem fenólicos são muito reativos quimicamente. Formam
pontes de hidrogênio intra e intermoleculares e um mol de tanino pode ligar-se a doze moles
de proteínas. Estes compostos são facilmente oxidáveis através de enzimas vegetais
específicas ou por influência de metais como cloreto férrico, que ocasiona o escurecimento de
suas soluções (MELLO et al., 2001; DUARTE et al., 2014).
1.2 Tanase
Tanino acil hidrolase (EC 3.1.1.20) ou simplesmente tanase (TAH) é uma enzima
extracelular envolvida na hidrólise de taninos. A TAH hidrolisa ésteres de taninos
hidrolisáveis (Fig. 2), produzindo moléculas de glicose e ácido gálico. A tanase pode ser
produzida na presença de ácido tânico por diversos micro-organismos como fungos
filamentosos, bactérias e leveduras (MADEIRA-JUNIOR et al., 2015).
Figura 2. Reação de hidrólise do ácido tânico, R1 (galoil) e R2 (digaloil) pela tanase
(AGUILAR; GUTIÉRREZ-SÁNCHEZ, 2001; BATTESTIN; MATSUDA; MACEDO, 2004).
Muitos autores relacionam a presença de taninos como um mecanismo de defesa dos
vegetais contra a ação microbiana. Em face disso, a produção de tanase pode ser considerada
como um contra-ataque às plantas por parte dos micro-organismos. A TAH atua na invasão da
planta hospedeira hidrolisando parte dos compostos fenólicos (taninos hidrolisáveis) presentes
nos tecidos vivos ou em decomposição (REDONDO et al., 2014).
A tanase geralmente apresenta pH ótimo entre 4.5-6.5, estabilidade ao pH na faixa de
3.5-8.0; além de temperatura ótima entre 30-50ºC, estabilidade térmica na faixa de 30ºC-70ºC
6
e, massa molecular entre 50kDa e 320kDa. Diferentes íons metálicos tem sido frequentemente
reportados como inibidores de tanase, tais como: íons de Fe3+
, Mg2+
, Mn2+
, Zn2+
e Cu2+
(PINTO et al., 2005). Além destes, metais pesados como Hg2+
, Co2+
, Ba2+
, Cd2+
, Ag+, Pb
+,
Sn2+
também são considerados potentes inibidores de tanase (YAO et al., 2014). O
comportamento da TAH em relação ao pH, temperatura e inibição por íons metálicos depende
basicamente das condições de cultivo e do micro-organismo utilizado na produção da enzima
(BENIWAL; CHHOKAR, 2010; CHÁVEZ-GONZÁLEZ et al., 2012). Dentre os fungos
filamentosos produtores de tanase, os gêneros Aspergillus e Penicillium são considerados os
melhores produtores, seja por fermentação em estado sólido ou fermentação submersa
(AGUILLAR et al., 2007; RENOVATO et al., 2011; CHÁVEZ-GONZÁLEZ et al., 2012).
1.3 Fontes de obtenção da tanase
A tanase foi primeiramente descrita por Knudson (1913), que descobriu a degradação
do ácido tânico por uma cepa de Aspergillus niger. Esta enzima pode ser produzida por
fermentação submersa e sólida, utilizando resíduos agroindustriais como fonte de carbono
(DE LIMA, et al., 2014; GONÇALVES et al., 2011; SOUZA et al., 2015). Poucos trabalhos
tratam da produção de tanase por fermentação submersa pois, esse tipo de fermentação é
menos viável em virtude da baixa produtividade da enzima tanase (PINTO et al., 2005). A
fermentação em estado sólido (FES) apresenta muitas vantagens em comparação com a
fermentação submersa, tais como: natureza extracelular da enzima, maior produtividade e
maior estabilidade às mudanças de pH e temperatura. Além disso, a FES oferece benefícios
econômicos e ambientais por utilizar resíduos agroindustriais como substrato (CHÁVEZ-
GONZÁLEZ et al., 2012).
A TAH não é igualmente ativa contra todos os taninos hidrolisáveis. As obtidas de
levedura são efetivas somente na decomposição do ácido tânico (galotanino). Já as TAH
bacterianas e de fungos filamentosos são eficientes na degradação de ácido tânico e outros
taninos hidrolisáveis que ocorrem na natureza (BHAT; SINGH; SHARMA, 1998). O
aumento da produção de tanase está intimamente relacionado com a disponibilidade de tanino
no meio, contudo, em altas concentrações de tanino o crescimento do fungo é inibido.
A produção de tanase pode ser realizada utilizando uma grande variedade de
substratos. Em folhas de chá verde como fonte de carbono, a produção da enzima foi maior
(3.6 U/g de substrato) do que utilizando folhas de Anacardium occidentale (1,59 U/g de
substrato) e 36 vezes maior do que a produção em folhas de Mangifera indica (VALERA;
7
JORGE; GUIMARÃES, 2015). Pesquisa realizada com resíduos de dendê e sementes de
tamarindo em pó para produção de tanase utilizando Aspergillus niger ATCC 16620, mostra
que os rendimentos máximos da enzima (13,03 UI/g) ocorreu após 96 horas de incubação e,
após o período de 120h, o rendimento da enzima reduziu para 6,44 Ul/g (SABU et al., 2005).
Kumar, Sharma e Singh (2007) produziram tanase através de Aspergillus ruber utilizando
como substrato folhas de jamelão (Syzygium cumini). Após 96 horas de fermentação os
autores observaram que a produção atingiu o valor de 69 U/g de enzima. Beniwal et. al
(2013), utilizaram serragem de Dalbergia sissoo para produção TAH através do Aspergillus
heteromorphus MTCC 8818. A produção máxima de 1,62 U/g de tanase ocorreu após 96h.
1.4 Gênero Aspergillus
As espécies de Aspergillus produzem um grande número de enzimas extracelulares e,
muitas delas são aplicadas na biotecnologia para degradar produtos e compostos. Dentre as
espécies produtoras de enzimas comercialmente importantes encontram-se: Aspergillus flavus,
A. niger, A. oryzae, A. nidulans, A. fumigatus, A. clavatus, A. glaucus, A. ustus e o A.
versicolor (SOARES et al., 2010; SCHUSTER et al., 2002). O gênero Aspergillus sp.
compreende mais de 260 espécies de fungos filamentosos. Podem apresentar colônias de
coloração branca, amarela, amarelo-esverdeada, amarronzada, preta ou verde. A cor da
colônia é a principal característica macroscópica utilizada para classificar as espécies deste
gênero. A forma, tamanho e ornamentação dos conídios também podem auxiliar na
identificação de isolados, no entanto, técnicas moleculares e bioquímicas são mais precisas.
Aspergillus são fungos ubíquos e anemófilos, classificados como os micro-organismos mais
abundantes, além de mundialmente distribuídos, podendo ser isolados do solo, ar, água,
alimentos, plantas, material em decomposição e superfícies (SAMSON; VARGA, 2009;
SIDRIM; ROCHA, 2004; WARD et al., 2006).
Os fungos constituem um grupo de microrganismos eucarióticos, uni ou
multicelulares, em geral multinucleados, com parede celular. Podem ser filamentosos,
constituídos por filamentos longos e ramificados denominados hifas ou leveduriformes,
constituídos por células individuais que se reproduzem por brotamento ou fissão binária
(STUART; PIMENTEL; MARCON, 2010). Nesse importante grupo de micro-organismos
mais de 77.000 espécies são conhecidas, sendo a maioria terrestre. Entre todos os grupos
fúngicos existentes, o filo Ascomycota tem sido cada vez mais estudado principalmente
devido ao seu potencial na produção de enzimas. Os ascomicetos são fungos filamentosos que
8
atuam na decomposição da matéria orgânica através da hidrólise das macromoléculas pelas
exozimas que secretam. Dentre estas enzimas encontram-se as amilases, pectinases, xilanases,
celulases, proteases e tanases que, apesar de serem importantes em vários seguimentos da
indústria, não são largamente explorada devido aos custos de seu processamento,
principalmente no que diz respeito à purificação (PUTZKE; PUTZKE, 2004).
1.5 Sistema de duas fases aquosas
O sistema de duas fases aquosa (SDFA) é uma tecnologia atraente para purificação de
biomoléculas por oferecer vantagens como: simples e rápida separação, clarificação do
extrato, baixa desnaturação devido ao alto teor de água em ambas as fases, rápida
transferência de massa, partição seletiva e baixo custo. Portanto, ele tem sido utilizado em
vários domínios da biotecnologia para separar as moléculas de interesse das moléculas
contaminantes (YUZUGULLU; DUMAN, 2015).
O primeiro sistema PEG/sal a ser utilizado pela indústria foi o sistema composto por
PEG/fosfato. Além de fosfato, outros sais como sulfatos e citratos, podem ser empregados em
sistema de duas fases aquosas (SILVA et al., 1999). O SDFA é formado pela mistura de dois
polímeros hidrófilos ou um polímero e um sal, em determinadas concentrações (ASENJO;
ANDREWS, 2011; ROSA et al., 2010). Após a homogeneização, cada componente do
sistema é concentrado em uma das fases, favorecendo, deste modo, a partição de
biomoléculas, tais como proteínas, células, fragmentos celulares ou ácidos nucléicos. A
estratégia básica de separação em SDFA baseia-se na predominante partição da molécula de
interesse para uma das fases do sistema e as contaminantes para a fase oposta (OLIVEIRA et
al., 2001). Neste sistema, as proteínas são divididas entre as duas fases com um coeficiente de
partição que pode ser modificado se as condições experimentais do meio como pH, sais, força
iônica e outros, forem alterados (BASSANI et al., 2010; SPELZINI et al., 2008).
O polietileno glicol (PEG) é um polímero vastamente utilizado em SDFA por ser uma
molécula inerte e de carga neutra que dificilmente desnatura proteínas (PEREIRA et al.,
2012). O sal citrato de sódio também é um composto desejável para formar o sistema de duas
fases pois ele é atóxico para humanos e biodegradável quando presente em rios, lagos e solo.
No SDFA, geralmente quase todas as biomoléculas menores tendem migrar para a fase
inferior (fase sal) que é mais polar. Considerando que as proteínas permanecem na fase
superior (fase PEG) menos polar, esta não é a ideal para a recuperação de proteínas. A fase
9
polimérica requer etapas adicionais como ultrafiltração e cromatografia que aumentaria o
custo do processo. (YUZUGULLU; DUMAN, 2015).
Os mecanismos que regem a partição de biomoléculas em um determinado SDFA
ainda não são totalmente compreendidos. Em geral, o particionamento de proteína é
impulsionado por Van der Waals, ligação de hidrogênio, hidrofóbicas e iônicas, interações
entre as biomoléculas e a fase circundante. Portanto, várias condições podem influenciar a
partição das macromoléculas, tais como: tamanho, carga, hidrofobicidade da molécula;
concentração e massa molar do polímero; tipo e concentração do sal utilizado; e, por fim, o
pH (NAGARAJA; IYYASWAMI, 2014).
Embora existam vários métodos disponíveis para a purificação de biomoléculas, estes
são por vezes considerados onerosos e de etapas complexas que resultam em perdas na
recuperação dos produtos biológicos. Por consequência, o interesse em técnicas mais
economicamente viáveis, como SDFA, e com menor número de etapas tem se tornado cada
vez mais atraente no tratamento de biomoléculas com aplicação industrial.
1.6 Aplicações da tanase
A biodegradação por determinados micro-organismos e enzimas é uma das maneiras
mais eficientes de degradar grandes moléculas de tanino em pequenas moléculas com elevado
valor. Os taninos apresentam efeitos antinutricionais bem conhecidos. Dependendo da
quantidade ingerida e do estado fisiológico do animal, os taninos podem causar diminuição na
disponibilidade de nutrientes e na produtividade animal, podendo levar à morte em alguns
casos (REDONDO et al., 2014). O uso de tanase em rações ricas em taninos pode trazer
efeitos benéficos na remoção desses compostos indesejáveis, favorecendo assim a
digestibilidade e aumentando a capacidade de absorção pelos animais (BATTESTIN;
MATSUDA; MACEDO, 2004).
Efluentes de curtumes contêm altas quantidades de polifenóis, o que representa um
potencial risco ao meio ambiente. A utilização de tanase pode constituir um tratamento
efetivo para esse tipo de efluente (AGUILAR; GUTIÉRREZ- SÁNCHEZ, 2001).
A hidrólise do ácido tânico pela tanase libera o ácido gálico, uma importante
substância que pode ser aplicada na indústria farmacêutica para a síntese de trimetoprima,
uma substância antibacteriana (SHETE; CHITANAND, 2015). Este ácido também pode ser
utilizado para síntese de propilgalato, um composto largamente utilizado como aditivo na
10
indústria de alimentos e como antioxidante em óleos e produtos ricos em lipídeos (KAR;
BANERJEE, 2000).
Na indústria de bebidas, a utilização de TAH dispensa o emprego de substâncias
químicas para eliminação de complexos insolúveis indesejados em chá instantâneo,
garantindo um produto final de excelente qualidade, solúvel em água e caracterizado pelo alto
conteúdo de componentes aromáticos e coloração desejada. A hidrólise dos polifenóis do
malte pela tanase faz com que não ocorra a descoloração e desenvolvimento de turbidez na
cerveja durante a estocagem (PINTO et al., 2005). Em média, 50% da coloração do vinho se
deve à presença de taninos. A oxidação destes componentes em contato com o ar pode causar
uma turbidez indesejável reduzindo a qualidade do produto final. Essa turbidez pode ser
evitada com o uso da tanase, que atua impedindo a oxidação (AGUILAR; GUTIÉRREZ-
SÁNCHEZ, 2001). A tanase também é utilizada como agente clarificador em alguns sucos de
frutas e em bebidas à base de café (SHARMA; CHATURVEDI; SHARMA, 2015). Sua
aplicação em chá verde tem sido recentemente estudada.
1.7 Chá verde (Camellia sinensis)
O princípio ativo das plantas medicinais é frequentemente relacionado a seus
compostos polifenólicos. No passado, os extratos de planta (chás) ricos em taninos eram
utilizados na medicina tradicional da China e Japão, para tratar diarréia, inflamações,
hemorragias, intoxicação por metais pesados e câncer (JANA et al., 2014).
Camellia sinensis é um arbusto da família Theaceae conhecida popularmente por: chá
verde, chá-da-Índia, banchá ou “green tea”. Os principais compostos químicos terapêuticos
do material vegetal C. sinensis, são polifenóis, que são potentes antioxidantes de radicais
livres, quelantes de metais e inibidores da lipoperoxidação, anti-inflamatórios,
antimicrobianos, inibidores da enzima conversora de angiotensina, auxiliam na prevenção da
osteoporose e podem contribuir na prevenção de câncer (SANTOS et al., 2014).
Para obtenção do chá, são utilizados as folhas secas e os brotos da planta. A
composição química dos chás pode variar quanto à espécie, idade das folhas, estação, clima
(umidade, temperatura, latitude) e condições de cultivo (solo, água, minerais, fertilizantes,
entre outros). Essas diferenças na matéria-prima refletem no sabor, cor e, possivelmente, nos
teores de flavonóides, que são utilizados para definir a qualidade da matéria prima vegetal
(PERON et. al. 2008; JAYASEKERA et al. 2011; FIMINO; MIRANDA, 2015). As
11
propriedades funcionais do chá estão relacionadas com o seu conteúdo polifenólico. Uma
bebida típica preparada como infusão (em água quente por 3 minutos) de 1 g de erva para 100
ml de água, contém geralmente entre 250-350mg de sólidos solúveis do chá, sendo 30-42%
do peso em catequinas e 3-6% em cafeína. No Brasil, o chá verde é comercializado
principalmente acondicionado em saquinhos de papel de filtro (sachê). Os estudos do chá
verde brasileiro (var. assamica) ainda são escassos quando comparados aos realizados com
chás verdes produzidos em outros países. Para que os benefícios do consumo da bebida sejam
máximos, são necessários estudos que assegurem as melhores formas de preparo, garantindo
maior extração e estabilidade de seus compostos bioativos (NISHIYAMA et al., 2010).
12
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WARD, O. P.; QIN, W. M.; DHANJOON, J.; YE, J.; SINGH, A. Physiology and
Biotechnology of Aspergillus. Advances in Applied Microbiology, v. 58, p. 75. 2006.
YAO, J. Production, characterization and applications of tannase. Journal of Molecular
Catalysis B: Enzymatic, v. 101, p. 137-147. 2014.
ZHANG, Y. et al. Improving the sweet aftertaste of green tea infusion with tannase. Food
Chemistry, v. 192, p. 470–476. 2016.
YUZUGULLU, Y.; DUMAN, Y. A. Aqueous Two Phase (PEG4000/Na2SO4) Extraction and
Characterization of an Acid Invertase from Potato Tuber (Solanum Tuberosum). Preparative
Biochemistry and Biotechnology, v. 7, p. 696-711. 2015.
17
CAPÍTULO 2
EXTRACTION IN AQUEOUS TWO-PHASE SYSTEM (PEG/CITRATE),
CHARACTERIZATION AND APPLICATION OF TANNASE FROM Aspergillus sp. SIS
25 IN GREEN TEA (Camellia sinensis)
Artigo a ser submetido à revista Fluid Phase Equilibria.
18
EXTRACTION IN AQUEOUS TWO-PHASE SYSTEM (PEG/CITRATE),
CHARACTERIZATION AND APPLICATION OF TANNASE FROM Aspergillus sp. SIS
25 IN GREEN TEA (Camellia sinensis)
Kátia K.S. Andrade Albuquerquea; Polyanna N. Herculano
b; Cynthia O. Nascimento
b; Daniela
A. Viana Marquesc; Romero M.P.B. Costa
b; Maria Luana S. Araújo
b; Kessia P. Souza
a;
Wendel Wagner C. Albuquerqueb; Ellen L. Clementino
b; Ana L.F. Porto
b,*
aCenter of Biological Sciences, Federal University of Pernambuco, 50670-901 Recife, PE, Brazil. bDepartment of Morphology and Animal Physiology, Federal Rural University of Pernambuco,
52171-900 Recife, PE, Brazil. cAcademic Unit of Serra Talhada, University of Pernambuco, 50750-500 Serra Talhada, PE,
Brazil. * e-mail: analuporto@yahoo.com.br
Highlights
• Purification using ATPS and application of tannase from Aspergillus in green tea.
• Liquid-liquid extraction of tanase using PEG/citrate ATPS.
• ATPS is an interesting method for purify the tannase.
Abstract
Tannase (EC 3.1.1.20) is an extracellular enzyme that hydrolyzes tannins producing gallic
acid and glucose. This enzyme is commercially important because presents applications in the
pharmaceutical industry, leather processing, animal feed, food and drinks. To purify enzymes
of commercial value, the aqueous two-phase system (ATPS) has been a cost-effective
alternative. In this work, tannase (TAH) from Aspergillus sp. SIS 25 has been studied in
aqueous two-phase system composed of polyethylene glycol (PEG) and sodium citrate and a
statistical design 23 was used to study the influence of molar mass of PEG (1000, 3350 and
6000), PEG concentration (CPEG) and sodium citrate concentration (CCIT), at pH 6.0. The
purified enzyme system was applied in green tea (Camellia sinensis) to assess their potential
to reduce undesirable compounds to drink. The tannase was preferentially partitioned to salt
phase of system once all the tests presented values of K less than 1. The effect of PEG molar
mass (MMPEG) and MMPEG-CPEG interaction were significant, both negative. The best
increase in purity (3.2) was observed in 8 test with 24% PEG 6000 and 20% salt. The
statistical model studied allowed partially purify tannase and also find other models that
promote improvements in the studied variables. The tannase obtained presented optimum
temperature at 30 °C and optimum pH 5.0; already the stability was lost at 50 °C. In all Na+
concentrations the enzyme was stimulated, however, in the presence of Zn2+
TAH was
completely inhibited. Surfactants no have significant influence on enzymatic activity, with
exception of Triton X-100 2% which decreased the relative of tannase activity by
approximately 50%. The tannase purified in ATPS on concentration of 0.75 mL hydrolysed
44% of phenolic compounds from green tea. Superior performance if compared with the
crude extract. Thus, this work provides subsidies for new studies that promote the purification
of tannase using ATPS, stressing the great biotechnological potential of this enzyme,
especially in green tea industry.
Keywords: aqueous two-phase systems, Aspergillus, purification, tannase, green tea.
19
1. INTRODUCTION
Tannin acyl hydrolase (EC 3.1.1.20) or tannase is an extracellular enzyme with great
biotechnological potential produced in the presence of tannic acid by various microorganisms,
especially filamentous fungi. Tannase (TAH) catalyzes the hydrolysis of tannins converting
them into gallic acid and glucose. Its application is well known in the food, pharmaceutical
and beverage, like teas [1,2].
Tea is one of the most popular and widely consumed beverages in the world and its
composition is rich in polyphenols which have antioxidant activity. Camellia sinensis (green
tea) is native to Southeast Asia and it is grown in more than thirty countries. Its extracts are
commonly used because of low cost and beneficial health effects, for example, in the
prevention of cancer, cardiovascular disease, and treating neurological disorders long term.
Green tea has also been used in diets in the form of teas and extracts or incorporated into
creams, gels, lotions and other pharmaceutical means [3,4].
As regards its use in tea, tannase reduces the adverse effects (bitter and astringent
taste) of the tannin in the beverage, enhancing sensory acceptance [5]. In the instant tea
production, TAH is used to remove the insoluble precipitates formed when the beverage is
cooled at temperatures below 4°C. These precipitates come from the interaction between
polymerized phenolic compounds and the caffeine. By degrading tannin, tannase prevents the
formation of those polymerized compounds, improving the quality of the tea (once the
enzymatic treatment, differently from the chemical treatment, preserves the desirable aromatic
compounds) [6].
In this process of applying enzymes for commercial purposes, the main restrictions on
the production of molecules with high levels of purity are the various steps required to
purification. These procedures, in general, are technically difficult and may lead to enzyme
denaturation, besides to require a high energy consumption and greater amount of chemicals
[7]. Thus, efforts should be concentrated on the development of new technologies to purify
enzymes with lower costs, in a sustainable way and preserving the conformational
compatibility of the biomolecules.
Aqueous two-phase system (ATPS) is a biocompatible method that allows the
partition and partial purification of biomolecules. The ATPS is usually created by the solution
of two immiscible hydrophilic polymers (natural or synthetic) or by the combination of a
polymer and a salt [8].
20
These systems compose an appropriate mean for the biomolecule extraction, once the
high water content in both phases (between 70 e 90%) provides an appropriate environment to
the activity of biologically active compounds, preserving their molecular stability and
allowing their processing. Currently, the process of separation and purification of bioproducts
is a very important segment for industries, representing 80% to 90% of the cost of production
[9]. Therefore, ATPS is an attractive method to the enzyme extraction.
Studies that allow the improvement of the extraction and purification of TAH by
aqueous two-phase system have received increased importance and impacted the cost-benefit
of the processes. The aim of this study is, therefore, to extract the tannase obtained from
Aspergillus sp.SIS 25 in ATPS PEG-citrate, to characterize the enzyme and applying it in
green tea (Camellia sinensis) from solid state fermentation, using coconut fiber substrate.
21
2. MATERIAL AND METHODS
2.1 Microorganisms
In this study, was used the filamentous fungi Aspergillus sp. SIS 25 isolated from
Caatinga soil, Serra Talhada, PE-Brazil.
2.2 Solid state fermentation and crude extract
To produce the tannase from Aspergillus sp. SIS 25, solid-state fermentation (SSF) was
performed using the coir as a substrate. The strain was maintained on Czapeck Dox Agar and
kept at 30 °C for 7 days. The inoculum was prepared by suspending spores from the Czapeck
Dox Agar plates in sterile 0.01% Tween-80 solution. The number of spores was determined in
a Neubauer counting chamber and 1 x 107 spores per mL were used to inoculate the
erlenmeyer flasks containing 10 g substrate used for SSF. Flasks were incubated at 30 °C for
48 h before harvesting. After fermentation, 18 mL of 10 mM sodium phosphate buffer (pH
5.5) was added to 3 g of the fermented mixture, and the maceration was performed. The
extract was clarified by filtration (Whatman no. 1 under vacuum) and centrifugation at 2000
rpm for 10 min. The supernatant was used as the crude enzymatic extract and was subjected to
enzymatic analysis and extraction of tannase in the ATPS.
2.3. Protein determination
Determination of total protein content of both the top and bottom phases of the
systems was carried out by spectrophotometrically using bicinchoninic acid following the
method described by Smith et al. [10], with absorbance measured at 595 nm. To avoid
interference from PEG and citrate, all samples were analysed against blanks containing the
same phase composition without proteins.
2.4 Tannase activity
The tannase activity was determined spectrophotometrically according to Sharma’s et
al. method [11] and modified by Ordoñez et al. [12], based on the formation of a chromogen
between gallic acid (released by the esterase activity of tannase) and rhodanine (2-thio-4-
ketothiazolidine). One unit of the enzyme was defined as micromole of gallic acid formed per
minute.
22
2.5 Preparation of aqueous two-phase systems
The systems were prepared with PEG of different molar mass (1000, 3350 and 6000
g/mol) and sodium citrate salt. Citric acid was added in an appropriate amount to maintain a
pH value of 6.0. The desired amounts of PEG and salt were placed in graduated tubes with
conical tips (15 mL). The crude extract containing tannase, which represents 20% of the total
system, was added to the tubes. Water was added to a final amount of 5 g. After addition of
all components of the system (PEG + citrate + water + crude extract) and vortex shaking for
1.0 min, the two phases were separated by settling for 60 min. The phase volumes were
measured, and the top and bottom phases were separately withdrawn with pipettes and
assayed for protein concentration and tannase activity.
2.5.1 Experimental design and statistical analysis
The influence of variables PEG molar mass (MMPEG), PEG concentration (CPEG)
and citrate concentration (CCIT) on variables results, purification factor (PF), activity yield
(Y) and partition coefficient (K), was evaluated from the results obtained by a 23 factorial
design, plus a central point, which was run in quadruplicate to allow estimation of the
experimental error [13]. The values selected for these variables (Table 1) were chosen based
on binodal diagrams reported in the literature [14]. All statistical and graphic analyses were
carried out with the aid of the Statistica 8.0 software (StatSoft Inc., Tulsa, OK, USA).
Table 1. Variable levels of the 23 experimental design selected for tannase extraction by
PEG/citrate ATPS.
2.5.2 Partition coefficient
The tannase partition coefficient was determined as the ratio of the enzyme activity in
the top phase (At) to that in the bottom phase (Ab):
(1)
Variables Low (-1) Central (0) High (+1)
PEG molar mass (g/mol) 1000 3350 6000
PEG concentration (%, w/w) 20.0 22.0 24.0
Citrate concentration (%, w/w)
15.0 17.5 20.0
b
t
A
AK
23
2.5.3 Activity yield
The activity yield was defined as the ratio of the total volumetric activity in the top
phase to that in initial extract and was expressed as percentage:
(2)
where Vt and Vi are the volumes of the bottom phase and the initial extract, respectively.
2.5.4 Purification factor (PF)
The purification factor was calculated as the ratio of the specific activity in the bottom
phase to the specific activity in the crude extract before partition (Ai):
CiAi
CbAbPF/
/ (3)
where Cb and Ci are total protein concentrations, expressed as mg/mL, in the bottom phase
and crude extract, respectively.
2.6 Enzymatic characterization
2.6.1 Effect and stability to temperature and pH influence on tannase activity
To determine the temperature optimum, enzyme assays were incubated at different
temperatures between 20 °C and 90 °C, with 10 °C interval. The thermal stability was
performed from the incubation of the enzyme at different temperatures (20 to 50 °C, with 10
°C interval) for 3 hours, aliquots withdrawn for analysis at 30 minute intervals.
The optimum pH for activity tannase purified in aqueous two-phase systems were
determined using different buffer solutions: sodium acetate (pH 3.0 to 5.0), Tris-HCl (pH 6.0
to 8.0) and glycine-NaOH (pH 9.0 and 10.0).
2.6.2 Effect of metal ions on tannase activity
The enzyme purification in ATPS was exposed to the following ionic solutions (5, 10
and 20 mM): calcium chloride [CaCl2], potassium chloride [KCl], sodium chloride [NaCl],
zinc chloride [ZnCl2], zinc sulfate [(ZnSO4) .7H2O], magnesium sulfate [MgSO4] and
100
AiVi
AtVtY
24
copper sulfate [CuSO4]. The enzyme was incubated at 30 °C for 30 minutes. The salts were
dissolved in Tris–HCl pH 7.75 with 0.15 M NaCl.
2.6.3 Surfactant influence on the activity of tannase
The influence of SDS, Triton X-100, Tween 20 and Tween 80 was studied in the
following concentrations: 0.5%; 1.0% and 2.0%. The enzyme purified in ATPS was exposed
to these surfactants and incubated at 30 °C for 30 minutes. The surfactants were dissolved in
Tris–HCl pH 7.75 with 0.15 M NaCl.
2.7 Hydrolysis of undesirable phenolic compounds in green tea by the action of the
enzyme tannase
Green tea was prepared using bulk sheets, following the methodology proposed by Lu
and collaborators [15]. For hydrolysis of phenols, 5 mL of tea was placed in test tubes with
different rates of pre-purified extract in ATPS (0.250 mL, 0.500 mL, 0.750 mL and 1.0 mL).
The tea without enzyme was used as control. The tubes were incubated at 30 °C for 120
minutes. The analyzes were performed every 30 minutes (30, 60, 90 and 120 min), applying
the Folin-Ciocalteu micro method to quantitate the levels of phenolic compounds of trials
[16]. The absorbance was read at 760 nm and gallic acid was used as standard for the
calibration curve. The extracts used contained 46.12 U/mL, 15.05 U/mL tannase in the crude
extract and partially purified, respectively.
25
3. RESULTS AND DISCUSSION
3.1 Tannase extraction in aqueous two-phase system
The strategy employed to achieve the aims of this study was to obtain linear models
describing the influence of the main variables: PEG molar mass (MMPEG), PEG
concentration (CPEG) and sodium citrate concentration (CCIT) on secondary variables:
partition coefficient (K), yield (Y) and purity factor (PF). The main experimental results on
extraction of tannase are listed in Table 2.
Table 2. Combinations of the levels of three independent variables (concentration of PEG
and sodium citrate and molecular weight of PEG) used in a complete factorial design 23 and
the values of the relative responses.
Run CPEG%
(p/p)
CCit%
(p/p)
MMPEG
g/mol PF K
Y (%)
1 20 15 1500 1,1 0,2 73,4
2 20 15 6000 0,86 0,1 50,3
3 24 15 1500 1,1 0,2 28,6
4 24 15 6000 1,5 0,2 95,7
5 20 20 1500 2,5 0,1 90,9
6 20 20 6000 1,7 0,2 76,4
7 24 20 1500 2,8 0,1 86,8
8 24 20 6000 3,2 0,1 93,6
9 (C) 22 17,5 3350 2,1 0,1 98,9
10 (C) 22 17,5 3350 1,8 0,1 93,0
11 (C) 22 17,5 3350 1,9 0,1 92,8
12 (C) 22 17,5 3350 2,0 0,1 92,5
CPEG% and CCIT%= PEG concentration and sodium citrate concentration, respectively; MMPEG = PEG
molar mass; PF= purification factor in the botton phase; K= partition coefficient; Y (%) = activity yield in
bottom phase.
The studied model showed good results in partial purification of tannase. The 8 test
was chosen as the best result for presenting the largest value of PF (3,2). This experiment was
comprised of higher concentrations of reactants: 24% PEG 6000 and 20% salt.
26
In all the tests one can see that the partition coefficient of the activity was lower than
1, indicating that most of the enzyme was extracted from the salt phase. The same was
observed by Nascimento and collaborators [17] using PEG/Citrate to purify lectin. Although
the partitioning efficiency depends on factors such as an electrical potential between the
phases, size and conformation of the molecule; the hydrophobic characteristic is considered
the most influential factor [18]. In a PEG/salt system partitioning can occur due to the effect
of "volume exclusion" in the polymer-rich phase or also cause the "salting out" effect in salt-
rich phase. The increasing in the salt concentration decreases the solubility of biomolecules in
the bottom phase (rich in salt) and propels them to the top phase. On the other hand, the
volume occupied by the polymers increases with the polymer concentration and its molecular
weight, promoting a decrease in the available space for the molecules in the upper layer, what
propels the molecules to the lower phase. [19,20].
The Pareto chart shows, in order of magnitude, the effects of variables and their
interactions, which are represented by names and numbers on the vertical axis. The length of
each bar is proportional to the standardized effect of the variable and the vertical line can be
used to judge the most important effects.
Figure 1. Pareto chart of the main effects and their interactions for the response variable K in
the tanase extraction process in ATPS PEG/Citrate using full statistical planning 23.
The Figure 1 shows that all terms were significant (at 95% confidence level) for the
variable K, for the values of the estimated effects with p <0.05. In order of magnitude, the
terms interaction between CPEG-CCIT and MMPEG were the most important effects, both
27
showing negative algebraic sign. Thus, decreasing CPEG, increasing CCIT and increasing
MMPEG, it is possible to obtain a better separation of the salt tannase phase.
Our reports are in agreement with the studies by Rodriguez-Duran et al. [21] which
have purified tannase obtained from Aspergillus niger by ATPS PEG/phosphate. The authors
used PEGs with molecular weights of 400, 600 and 1000, and the results showed that by
increasing MMPEG significantly there is a consequent decrease in the enzyme partition
coefficient. Also according to those authors, the hydrophobic proteins have high K values of
activity. Based on this, the authors concluded that the TAH of Aspergillus niger has few
hydrophobic areas on its surface since all values of K activity were smaller than 1
(corroborating our results), suggesting that the tannase has a hydrophilic nature. A significant
and positive effect on the interaction of MMPEG-CCIT variables was observed. This means
that the simultaneous increase of these two variables will displace a better partitioning of the
enzyme in bottom phase.
Figure 2. Pareto chart of the main effects and interactions for variable Yeld (%) in the tanase
extraction process in ATPS PEG/Citrate using full statistical design 23, in bottom phase.
The effect of main variables and their interactions on the response variable Y(%) can
be seen in Figure 2. All positive significant terms indicate that increasing the variable
promotes better recovery at the salt phase. This occurs with increasing CCIT, simultaneous
increase in MMPEG-CPEG and increased MMPEG, as shown in the graph. Contrary to what
28
is observed for the variable K, not all effects were significant at the 95% confidence level.
CPEG-CCIT and CPEG not presented p <0.05. Although the effect of the main variable
CPEG was not significant at the 95% confidence level, the interaction of this term with
MMPEG shows that in joint action, this variable may prove significant effect for Y(%).
With ANOVA, the linear model for the yield response variable elucidated 70%
(R2=0,70) of the results obtained in the assays. Some misfit for the model was observed, but
with low error of 0.30 at a confidence level of 95%.
3.2 Effect of temperature and pH on tannase activity
The optimum temperature of tannase was observed at 30 °C, in which the enzyme had
100% of its efficiency (Figure 3A).
Figure 3. Influence of different temperatures in the activity of tannase produced by
Aspergillus sp. 25 SIS (A) and enzyme stability for 3 hours of incubation (B).
The increase in temperature caused gradual loss in activity of the molecule; at 90 °C,
for example, the enzyme lost 71% of its activity. The tanase remained stable at its optimum
29
temperature for more than 3 hours. At 50 °C the enzyme began to lose stability since its
relative activity began to decrease (Figure 3B).
The optimum pH of tannase was observed between 5.0-6.0, in which the enzyme
showed 100% and 96% of its activity, respectively (Figure 4), when it was incubated at 30 °C
in acetate buffer sodium. Significant activities were also observed at pH's 3.0; 4.0 and 7.0. In
an alkaline pH it was verified that the activity of the enzyme decreased significantly, reaching
44% in NaOH-glycine buffer (pH 10).
Figure 4. Influence of different pH in the activity of tannase produced by Aspergillus sp. SIS
25 after 30 minutes of incubation.
Microbial tannase generally has the optimum temperature ranges of 20-60 °C and
thermostability between 30 and 60 °C [22]. As in this study, Mahapatra et al. [23] They
described how great a temperature of 30 °C to tannase different Aspergillus species.
Similarly, Costa et al [24] also observed an optimum temperature of 30-35 °C to A. tamarii
tannase, which is stable for more than 2 hours at 40 °C, completely lose their stability at
temperatures higher than 45 °C. Likewise, the tannase from Aspergillus niger ATCC 6514.07
showed enhanced activity around 35 °C and pH 6.2 [25]. In line with most of the work
described herein, Jana et al. [26] observed an immobilized tannase of Bacillus subtilis PAB2
that having optimum activity at 40 °C, at pH 5.0, similar to its free form, being stable over a
wide pH range (3.0-8.0).
Enzymes are very sensitive to changes in pH and work best on a very limited range
[27]. As the tannase from Aspergillus SIS 25, the tannase Penicillium variable was reported to
be stable in a pH range of 4.0-6.0 therefore showed that almost 100% activity for 24 hours
30
[28]. Tannase of A. tamarii studied by Costa et al. [24] also showed pH characteristics
relatively similar to the enzyme of the present work. The same presented optimum pH 5.0
with substantial activity at pH 4.0 to 8.0, and is stable over a wide pH range (3.0 to 8.0).
Many other acidophilic nature of tannase with optimum pH similar to that observed in this
study are reported in the literature, such as A. awamori tannase and P. variable with pH 5.0
[23,28] and pH 6.0 tannase obtainable from A. niger [29].
The optimum pH acid suggests applicability in the food industry mainly from fruit,
where the acidity favors the enzyme activity [30]. The same principle can also be practiced in
processing beverages such as green tea, which has a pH of about 6.0, which favors the
catalysis of undesirable compounds such as tannins.
3.3 Influence of surfactants on the enzyme activity
In the presence of Tween 20, the enzyme activity remained unchanged showing that
the molecules of the surfactant concentrated at 0.5% and 1% did not interfere with the
accessibility of the substrate to the active site of the enzyme (Table 3).
Table 3. Influence of various surfactants on tannase enzyme activity.
In the presence of SDS and Tween 80 surfactan, the enzyme lost its activity especially
in higher concentrations. Although, Triton X-100 2% had greater interference with the
binding of substrate, decreasing the relative activity to 46.69%.
Surfactants are substances that can denature proteins and therefore play an important
role in the catalytic activity of enzymes. Their effects on the catalytic ability of tanase vary
considerably [22]. Unlike the present study, a significant loss of activity in the presence of
Surfactant Concentration (%) Relative activity (%)
Tween 20 (% v/v)
0,5 105,37
1 99,29
2 85,89
Tween 80 (% v/v)
0,5 79,28
1 62,27
2 55,96
Triton X-100 (% v/v)
0,5 64,81
1 61,86
2 46,69
SDS (mM)
0,5 65,76
1 70,54
2 66,76
31
Tween 20 was reported to tannase Verticillium sp. P9 [31], while small positive effect was
observed for tannase from Aspergillus niger GH1 [32]. Tannase activity of Penicillium
variable and Aspergillus foetidus were completely inhibited by SDS and Tween 80 [28,33],
different this work, where there was observed complete inhibition by any of the surfactants.
With this, it is clear that the tannase from Aspergillus SIS 25 has a certain resistance to most
surfactants, seen here as tannase denaturing agents.
3.4 Effect of metal ions on the enzyme activity
More than 75% of the enzymes require metal ions to express its maximum catalytic
ability. At low concentrations, some metals may act as cofactors which enhance enzymatic
activity but at high concentrations, what happens is an inhibition [32].
They tested different concentrations of metal ions that in the literature as inhibitors or
stimulators of the tannase activity, as can be seen in Figure 5. Tannase from Aspergillus sp.
SIS 25 was resistant to most of the studied ions. The enzyme showed maximum activity in the
presence of Na+ and Mg
2+, lost about 40% activity in the presence of Cu
2+ but was Zn
2+ that
completely inhibited the tannase action.
Figure 5. Influence of various metal ions concentration on tannase activity of Aspergillus sp.
SIS 25, extracted in aqueous two-phase system.
The inhibitory effects of Fe3+
, Cu2+
and Zn2+
have been frequently reported in the
literature. The tannase A. niger GH1, for example, was strongly inhibited by Cu2+
and Zn2+
by
slightly inhibited, in accordance with Mata-Gómez et al [32]. However, other strains of A.
niger has produced tannase strongly inhibited by Mg2+
and Mn2+
, as the tannase from
32
Aspergillus niger ATCC 16620 [34] and Aspergillus niger ITCC 6514.07 [25] have shown
that the presence of magnesium cations. In contrast, tannase Verticillium sp. was inhibited by
Mn2+
, Zn2+
and Cu2+
however, activated by Mg2+
[31], as well as TAH seen in this work and
tannase Rhizopus oryzae, Aspergillus foetidus [35] and Aspergillus awamori MTCC 9299
[36].
Cofactors are usually not required for the tannase activity, but divalent cations, such as
magnesium, often stimulate the enzyme activity. This probably happens due to a variety of
mechanisms, including activation by metal ions, altering the equilibrium constant of the
enzyme reaction, or causing a change in the surface charge of the enzyme. Furthermore, the
tannase activity is generally inhibited by heavy metals such as Hg2+
, Co2 +
, Ba2 +
, Cd2 +
, Ag+,
Pb2+
, Sn2+
[22].
3.5 Hydrolysis of undesirable phenolic compounds in green tea by the action of the
enzyme tannase
The aqueous two-phase system is a method of partial purification which
simultaneously clarifies the enzymatic extract (Figure 6.A).
Figure 6. Pigment retention in the PEG phase (top) of the ATPS (A) and qualitative
difference in color of green tea (1), green tea treated with partially purified tannase (2) and
green tea with crude extract (B).
The retention of undesirable components (such as pigments) in this system facilitates
the use of the enzyme in various applications such as green tea, as shown in Figure 6.B.
The action of crude enzymatic extract and purified enzyme in ATPS on hydrolysis of
green tea compounds it is represented in the Table 4. The hidrolyzes was tested at different
concentrations of the crude extract and of the purified enzyme in ATPS, in different time
intervals. The control (tea without enzyme) initially contained 5.58 U /ml of total phenolics.
In tea sample treated with crude extract there was an initial increase of phenolic compounds,
33
in relation to control, due to the presence of contaminants from phenols extract. Then the
reduction of phenols was observed over time, possibly due to a greater exposure of tannins the
presence of tannase. The initial increase of phenols shows that contaminants from the crude
extract are able to interfere with the tannins hydrolysis process, contributing to the emergence
of undesirable results in tea as intensifying color and astringent taste.
Table 4. Effect of concentration of 0.75 mL of crude extract and 0.75 mL of purified tannase
enzyme in ATPS (PEG /Citrate) on hidrolyzes of 1mL green tea phenolic compounds.
Hydrolysis of phenols extracted from the tannase in ATPS showed gradual reduction
of the compounds in relation to control, with each increase of enzyme concentration. The best
result was observed after 2 hours incubation with 0.75 mL of tannase from ATPS at 30 °C,
wherein the content of phenolic compounds in the tea was reduced to 56% (3.14 U / mL). At
this same time interval, green tea sample with 0.75 ml of crude extract still had 7.2 U/mL total
phenols, equivalent to 130%. In the presence of the highest concentration (1 mL) of purified
enzyme, the phenols remained at an average 68% reduction of 32%. The 0.25 mL and 0.50
mL concentrations showed the smaller reduction of phenolic compounds: 16% and 24%,
respectively.
Few studies on hydrolysis of phenolic compounds by tanase are reported in the
literature. The existing works mainly deals about the action of the enzyme in the process of
clarification of fruit juice. Sharma et al (2014) tested the activity of tannase produced by
Aspergillus niger in the detanification of guava juice, using tanase at 2%. After a period of 60
minutes, the authors verified a decrease of 59.23% in the beverage tannin content. Lima et al.
(2014) using tannase from Penicillium montanense for clarifying grape juice, was able to
Assay Time (min) Total phenols (%)
Green tea treated with
0.75 mL of crude
extract
30 137
60 137
90 132
120 130
Green tea treated with
0.75 ml of purified
enzyme by ATPS
30 75
60 71
90 64
120 56
34
reduce 46% of tannin content after 2 hours of incubation at 37 °C with 1 mL of crude enzyme
extract.
The fact that the enzymes possess specific substrates favors the understanding that the
phenolic compounds reduced in green tea are actually tannins. This reduction, which can be
followed by quantification of total phenols, shows that it is possible to extract in ATPS one
tanase with promising use in biotechnology. Tannase from system when applied to green tea
showed superior performance compared to the crude enzyme extract, suggesting the
importance of further studies to optimize its purification and consequent use in the industry.
Thus, this work confirms the potential of the ATPS as an economically viable method for
purification of tannase, making than enzyme promising on improvement of sensory aspects of
green tea.
35
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38
CONSIDERAÇÕES FINAIS
A melhor extração de tanase em sistema de duas fases aquosas ocorreu no ensaio
composto por 24% de PEG 6000 e 20% de citrato de sódio, no qual foi obtido um aumento de
pureza (AP) de 3,2. A partir dos efeitos das variáveis independentes sobre as variáveis
resposta é possível descrever um melhor modelo estatístico para a extração da enzima de
interesse. A massa molar do PEG e a interação entre MMPEG-CPEG apresentou influência
negativa na partição da molécula entre as fases do sistema. Isso implica dizer que o aumento
da MMPEG resultará em valores melhores do coeficiente de partição, para extrair a enzima
tanase na fase sal.
A tanase de Aspergillus sp. SIS 25 apresentou máxima atividade a 30 °C e em pH 5,0
porém, perdeu estabilidade a 50 °C. Quanto ao efeito de íons metálicos foi observado uma
interessante resistência à maioria dos íons. O Na+ potencializou a atividade da enzima e o
Mg2+
, frequentemente descrito como inibidor de tanase, não interferiu em sua atividade. Já o
íon Zn2+
mostrou-se um potente inibidor de tanase, zerando completamente sua atividade.
Não foram observadas reduções significativas na atividade da TAH quando esta foi exposta à
maioria dos surfactantes. Em exceção, o Triton X-100 a 2% reduziu pela metade o potencial
catalítico da tanase. A TAH desse trabalho também apresentou resultados interessantes
quando aplicada em chá verde. A enzima purificada em SDFA foi capaz de reduzir 44% dos
compostos fenólicos indesejáveis, apresentando-se mais viável nessa aplicação se comparada
à enzima no extrato bruto.
Os resultados aqui apresentados confirmam que o SDFA é um método interessante
para purificar parcialmente enzimas de interesse comercial como a tanase e, fortalece o
potencial uso dessa molécula na hidrólise de taninos presentes no chá verde, promovendo
novos estudos que explorem o uso biotecnológico dessa enzima.
39
ANEXO I
NORMAS DA RESVISTA
40
FLUID PHASE EQUILIBRIA An International Journal
AUTHOR INFORMATION PACK
TABLE OF CONTENTS . . • Description p.1 • Audience p.2
• Impact Factor p.2
• Abstracting and Indexing p.2
• Editorial Board p.2
• Guide for Authors p.4
ISSN: 0378-3812
DESCRIPTION . Fluid Phase Equilibria publishes high quality papers dealing with experimental,theoretical and applied research related to equilibrium and transport properties of fluid and solid phases. The fluid phase properties of interest include: PVT, enthalpies, heat capacities, Joule-Thomson coefficients, Gibbs and Helmholtz energies, chemical potentials, activity and fugacity coefficients, critical properties, chemical equilibria, multiphase equilibria and interfacial properties, thermal conductivity, viscosity and rheological properties, and diffusion coefficients. A wide range of pure and mixed fluids may be considered: Non-polar and polar small organic and inorganic molecules, ions, metals, polymers, surfactants, ionic liquids, gas hydrates, complex and biological molecules (e.g. proteins). Fluids should be well-characterized with respect to composition, or be specified with sufficient information for the experimental results to be reproduced (e.g. analysed by up-to-date techniques, or mixtures that can be obtained through a well-established published protocol). Experimental measurements: Unless they are accompanied by contemporary or new theory, papers will be refused if they report experimental data only at pressures and temperatures close to ambient on any of the following liquid or liquid mixture properties: viscosity; density; speed of sound; refractive index; surface tension. Similarly, papers will be refused if they only report phase equilibrium compositions, such as solubilities, at conditions near ambient without theoretical analysis and interpretation. All data reports and analyses will be examined by NIST for consistency with the requirements posted at http://trc.nist.gov/FPE-Support.html Theoretical and modeling studies: Theoretical techniques may be chemical thermodynamics, applied statistical mechanics, molecular physics, molecular simulation, quantum chemistry, applied mathematics.
41
Papers with new models, or modifications of available models, are expected to show comparisons for accuracy and predictive ability with applicable data and contemporary existing models.
All modeling of properties and phenomena based on artificial neural networks, machine
learning algorithms, and similar information processing approaches will only be considered
when comparisons of accuracy are made with existing physically-based models or if no
thermodynamic models are available. Further, the work must describe the procedure well
enough that readers may be able to independently reproduce the results.
Systems containing surfactants must be associated with the thermodynamic and transport properties described above, with relevant complex substances such as asphaltenes or ionic liquids, or with separation processes. Fundamental studies focused strictly on micellization or micelle structure will be refused.
AUDIENCE . Researchers and Applied Scientists, particularly those in chemical and metallurgical engineering, concerned with the properties or applications of fluid phase equilibria.
IMPACT FACTOR . 2014: 2.200 © Thomson Reuters Journal Citation Reports 2015
ABSTRACTING AND INDEXING . ASCA Chemical Engineering Biotechnology Abstracts Current Contents/Engineering, Computing & Technology Current Contents/Physics, Chemical, & Earth Sciences Engineering Index GEOBASE INSPEC Physics Abstracts Science Citation Index Scopus
EDITORIAL BOARD . Editor-in-Chief C. McCabe, Dept. of Chemical & Biomolecular Engineering, Vanderbilt University, Nashville, Tennessee, USA Editors G. Kontogeorgis, Dept. of Chemical and Biochemical Engineering, Danmarks Tekniske Universitet (DTU), Soltofts Plads, Building 229, DK-2800, Lyngby, Denmark J.P. O'Connell, University of Virginia, Dept. of Chemical Engineering, 102 Engineers' Way, VA 22904-4741, Charlottesville, Virginia, USA A.M. Soto, Dept. of Chemical Engineering, School of Engineering, Universidade de Santiago de Compostela, Rúa Lope Gómez de Marzoa s/n, E-15706, Santiago de Compostela, Spain
42
Editorial Board C. Adjiman, Dept. of Chemical Engineering, Fac. of Engineering, Imperial College London, London, SW7 2AZ, UK, South Kensington Campus S. Bottini, Planta Piloto de Ingeniería Química (PLAPIQUI), Camino La Carrindanga, Km 7, 8000, Bahía Blanca, Argentina C.-C. Chen, Dept. of Chemical Engineering, Texas Tech University, 6th and Canton, Lubbock, 79409, Texas, USA P.T. Cummings, Dept. of Chemical Engineering, Vanderbilt University, VU Station B, Box 351604, Nashville, TN 37235-1604, Tennessee, USA V. Dohnal, Dept. of Physical Chemistry, Institute of Chemical Technology, Technická 5, 16628, Prague 6, Czech Republic R. Dohrn, Property Data & Thermodynamics, BTS-TD-DP-PDT, Bayer Technology Services GmbH, D-51368, Leverkusen, Germany I. Economou, Chemical Engineering Program, 336B Texas A&M Engineering Building, , Texas A&M University at Qatar, Education City, PO Box 23874, Doha, Qatar S. Enders, Chair of Thermodynamics and Thermal Separation Science, BH 7-1, Technische Universität Berlin (TUB), Ernst-Reuter Platz 1, , 10587, Berlin, Germany E. Filipe, Departmento de Engenharia Química, Centro de Química Estrutural, Instituto Superior Técnico, 1049-001, Lisboa, Portugal H. Inomata, Research Ctr. of Superciritcal Fluid Technology, Tohoku University, 404-11-6-6 Aoba, Aramaki, Aoba-ku, 980-8579, Sendai, Japan Y. Iwai, Dept. of Chemical Engineering, Kyushu University, 744, Motooka, 819-0395, Nishi-ku, Fukuoka, Japan X.-H. Lu, Dept. of Chemical Engineering, Nanjing University of Science and Technology, No.5, Xin Mo Fan Ma Lu, 210009, Nanjing, China E. Maginn, Dept. of Chemical Engineering, University of Notre Dame, 180 Fitzpatrick Hall, Notre Dame, IN 46556, Indiana, USA G. Maurer, Fachbereich Maschinenbau und Verfahrenstechnik, Lehrstuhl fur Technische Thermodynamik, Technische Universität Kaiserslautern, Erwin-Schrodinger-Strasse, Gebausde 44, 67653, Kaiserslautern, Germany J. Moore, 1702 Building, Office 300E, The Dow Chemical Company, Midland, 48674, Michigan, USA C. Panayiotou, Dept. of Chemical Engineering, Aristotle University of Thessaloniki, GR-54124, Thessaloniki, Greece J.M. Prausnitz, Dept. of Chemical and Biomolecular Engineering, University of California at Berkeley, 201, Gilman Hall, Berkeley, CA 94720-1462, California, USA D. Richon, Dept. of Biotechnology and Chemical Technology, School of Chemical Technology Aalto University, FI-00076, Aalto, Finland G. Sadowski, Laboratory for Thermodynamics, Technische Universität Dortmund, Emil-Figge-Strasse 70, 44227, Dortmund, Germany J.I. Siepmann, Dept. of Chemistry, University of Minnesota, 207 Pleasant St. SE, Minneapolis, MN 55455-0431, Minnesota, USA A.I. Victorov, Dept. of Chemistry, St. Petersburg State University, 26 Universitetsky prosp., Petrodvoretz, 198504, St. Petersburg, Russian Federation W. Wang, College of Chemical Engineering, Research Center of the Ministry of Education for High Gravity Engineering and Technology, Beijing University of Chemical Technology, 15 Beisanhuandonglu, 100029, Beijing, China
43
GUIDE FOR AUTHORS . Your Paper Your Way We now differentiate between the requirements for new and revised submissions. You may choose to submit your manuscript as a single Word or PDF file to be used in the refereeing process. Only when your paper is at the revision stage, will you be requested to put your paper in to a 'correct format' for acceptance and provide the items required for the publication of your article. To find out more, please visit the Preparation section below. Editorial and Introduction Editorial New procedures for articles reporting thermophysical properties Fluid Phase Equilibria, along with other journals in the field, established collaboration with the Thermodynamics Research Center (TRC) of the National Institute of Standards and Technology (NIST) in 2009 for the purpose of ensuring the quality of published experimental data. In a joint statement [1], the editors of the five journals involved set out the rational for the cooperation in terms of helping to ensure that authors and reviewers were made aware of any previously-published literature values for the properties and systems in question. The process involved NIST 'capturing' the new experimental data, comparing it against existing values in the NIST data archive and providing a report that: (a) listed relevant literature sources; and (b) highlighted any obvious discrepancies in the new data. In order to streamline the process and to further enhance the quality of published articles, we are now introducing one change to the way in which the NIST cooperation is implemented. Effective in February 2013, responsibility for preparing a Literature Report will shift from NIST to the submitting authors. Submitting authors will be able to prepare their own Literature Report by using ThermoLit, a publicly available (http://trc.nist.gov/thermolit/) program. This will eliminate NIST's role in providing this report, and thus speed the review process and provide added benefit to authors who will have literature citation results on hand at a stage when they can do the most good. Please, note that use of ThermoLit is designed as an aid to the traditional required literature review and must not be used as a substitute. NIST will continue to provide a data evaluation at the end of the review process, immediately prior to final acceptance of the article. This data evaluation will compare the reported experimental data with that existing in the NIST Data Archive and highlight any unexpectedly large discrepancies, such as those arising from typographical errors. Though the data evaluation step has not changed, we will use this opportunity for a reminder that experimental results and their uncertainties must be tabulated in the way described in the Guide for Authors. A key feature is that tables be self-contained and include the uncertainties of all reported quantities (variables, constraints, and properties). In addition, we have incorporated new standards relating to the description of chemical samples and we encourage authors to present details of their samples in an easily-readable tabular form. To assist authors, a large number of example tables have been prepared by NIST and are available (http://trc.nist.gov/FPE-Support.html). The new procedures will provide literature citations to authors before submission of their manuscript and speed the review process. Indeed, authors are encouraged to use ThermoLit in advance of experiments to help minimize duplication of effort. In 2012, new IUPAC guidelines for the reporting of phase equilibrium measurements were published (Pure Appl. Chem. 2012, 84(8), 1785-1813), and the requirements of this journal are consistent with these recommendations.
44
Prior to submission, authors are strongly encouraged to review a checklist based on these recommendations, which is available (http://trc.nist.gov/FPE-Support.html). We are certain that the new Literature Report tool and the procedures described here will further enhance the already high quality of articles published in Fluid Phase Equilibria. Th.W. de Loos, Editor Clare McCabe, Editor J.P. O'Connell, Editor
References 1. P.T. Cummings, Th.W. de Loos, J.P. O'Connell, Fluid Phase Equilibria 276 (2009) 1165-1166. Aims and Scope Fluid Phase Equilibria publishes high quality papers dealing with experimental, theoretical and applied research related to equilibrium and transport properties of fluid and solid phases. The fluid phase properties of interest include: PVT, enthalpies, heat capacities, Joule-Thomson coefficients, Gibbs and Helmholtz energies,
chemical potentials, activity and fugacity coefficients, critical properties, chemical equilibria,
multiphase equilibria and interfacial properties, thermal conductivity, viscosity and diffusion
coefficients. A wide range of pure and mixed fluids may be considered: Non-polar and polar small organic and inorganic molecules, ions, metals, polymers, surfactants, ionic liquids, gas hydrates, complex and biological molecules (e.g. proteins). Fluids should be well-characterized with respect to composition, or be specified with sufficient information for the experimental results to be reproduced (e.g. analysed by up-to-date techniques, or mixtures that can be obtained through a well-established published protocol). Experimental measurements: Unless they are accompanied by contemporary or new theory, papers will be refused if they report experimental data only at pressures and temperatures close to ambient on any of the following liquid or liquid mixture properties: viscosity; density; speed of sound; refractive index; surface tension. Similarly, papers will be refused if they only report phase equilibrium compositions, such as solubilities, at conditions near ambient without theoretical analysis and interpretation. All data reports and analyses will be examined by NIST for consistency with the requirements posted at http://trc.nist.gov/FPE-Support.html Theoretical and modeling studies: Theoretical techniques may be chemical thermodynamics, applied statistical mechanics, molecular physics, molecular simulation, quantum chemistry, applied mathematics. Papers with new models, or modifications of available models, are expected to show comparisons for accuracy and predictive ability with applicable data and contemporary existing models. All modeling of properties and phenomena based on artificial neural networks, machine learning algorithms, and similar information processing approaches will only be considered when comparisons of accuracy are made with existing physically-based models or if no thermodynamic models are available. Further, the work must describe the procedure well enough that readers may be able to independently reproduce the results.
45
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reuse • An open access publication fee is payable by authors or on their behalf e.g. by their research funder or institution Subscription • Articles are made available to subscribers as well as developing countries and patient groups through our universal access programs (https://www.elsevier.com/access). • No open access publication fee payable by authors. Regardless of how you choose to publish your article, the journal will apply the same peer review criteria and acceptance standards. For open access articles, permitted third party (re)use is defined by the following Creative Commons user licenses: Creative Commons Attribution (CC BY) Lets others distribute and copy the article, create extracts, abstracts, and other revised versions, adaptations or derivative works of or from an article (such as a translation), include in a collective work (such as an anthology), text or data mine the article, even for
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commercial purposes, as long as they credit the author(s), do not represent the author as endorsing their adaptation of the article, and do not modify the article in such a way as to damage the author's honor or reputation. Creative Commons Attribution-NonCommercial-NoDerivs (CC BY-NC-ND) For non-commercial purposes, lets others distribute and copy the article, and to include in a collective work (such as an anthology), as long as they credit the author(s) and provided they do not alter or modify the article. The open access publication fee for this journal is USD 2100, excluding taxes. Learn more about Elsevier's pricing policy: https://www.elsevier.com/openaccesspricing. Green open access Authors can share their research in a variety of different ways and Elsevier has a number of green open access options available. We recommend authors see our green open access page for further information (http://elsevier.com/greenopenaccess). Authors can also self-archive their manuscripts immediately and enable public access from their institution's repository after an embargo period. This is the version that has been accepted for publication and which typically includes author-incorporated changes suggested during submission, peer review and in editor-author communications. Embargo period: For subscription articles, an appropriate amount of time is needed for journals to deliver value to subscribing customers before an article becomes freely available to the public. This is the embargo period and it begins from the date the article is formally published online in its final and fully citable form. This journal has an embargo period of 24 months. Elsevier Publishing Campus The Elsevier Publishing Campus (www.publishingcampus.com) is an online platform offering free lectures, interactive training and professional advice to support you in publishing your research. The College of Skills training offers modules on how to prepare, write and structure your article and explains how editors will look at your paper when it is submitted for publication. Use these resources, and more, to ensure that your submission will be the best that you can make it.
Language (usage and editing services) Please write your text in good English (American or British usage is accepted, but not a
mixture of these). Authors who feel their English language manuscript may require
editing
to eliminate possible grammatical or spelling errors and to conform to correct scientific
English may wish to use the English Language Editing service available from Elsevier's
WebShop (http://webshop.elsevier.com/languageediting/) or visit our customer support
site (http://support.elsevier.com) for more information. Submission The only method of submission to this journal is through the online Elsevier Editorial
System (EES). Submission to this journal proceeds totally online. Use the following
guidelines to prepare your article. Via the online submission site of this journal
(http://ees.elsevier.com/fluid) you will be guided stepwise through the creation and
uploading of the various files. The system automatically converts source files to a single
Adobe Acrobat PDF version of the article, which is used in the peer-review process.
Please note that even though manuscript source files are converted to PDF at submission
for the review process, these source files are needed for further processing after
acceptance. All correspondence, including notification of the Editor's decision and
requests for revision, takes place by e-mail and via the author's homepage, removing the
need for a hard-copy paper trail. Special instructions for manuscripts reporting experimental results
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Referees Please submit the names, full affiliations (department, institution, city and country) and email
addresses of five potential Referees. Appropriate reviewers should be knowledgeable about
the subject but have no close connection with any of the authors. At least three reviewers
must be from outside the lead author's geographical region. Suggested reviewers must not be
former co-authors or colleagues and must be from institutions other than those of any of the
Authors. You may also name reviewers that you do not want to review your manuscript and
state your reasons for doing so. PREPARATION NEW SUBMISSIONS Submission to this journal proceeds totally online and you will be guided stepwise through the creation and uploading of your files. The system automatically converts your files to a single PDF file, which is used in the peer-review process. As part of the Your Paper Your Way service, you may choose to submit your manuscript as a single file to be used in the refereeing process. This can be a PDF file or a Word document, in any format or lay-out that can be used by referees to evaluate your manuscript. It should contain high enough quality figures for refereeing. If you prefer to do so, you may still provide all or some of the source files at the initial submission. Please note that individual figure files larger than 10 MB must be uploaded separately. References There are no strict requirements on reference formatting at submission. References can be in any style or format as long as the style is consistent. Where applicable, author(s) name(s), journal title/book title, chapter title/article title, year of publication, volume number/book chapter and the pagination must be present. Use of DOI is highly encouraged. The reference style used by the journal will be applied to the accepted article by Elsevier at the proof stage. Note that missing data will be highlighted at proof stage for the author to correct. Formatting requirements There are no strict formatting requirements but all manuscripts must contain the essential elements needed to convey your manuscript, for example Abstract, Keywords, Introduction, Materials and Methods, Results, Conclusions, Artwork and Tables with Captions. If your article includes any Videos and/or other Supplementary material, this should be included in your initial submission for peer review purposes. Divide the article into clearly defined sections. Figures and tables embedded in text Please ensure the figures and the tables included in the single file are placed next to the relevant text in the manuscript, rather than at the bottom or the top of the file. REVISED SUBMISSION Use of word processing software Regardless of the file format of the original submission, at revision you must provide us with
an editable file of the entire article. Keep the layout of the text as simple as possible. Most
formatting codes will be removed and replaced on processing the article. The electronic text
should be prepared in a way very similar to that of conventional manuscripts (see also the
Guide to Publishing with Elsevier: https://www.elsevier.com/guidepublication). See also the
section on Electronic artwork. To avoid unnecessary errors you are strongly advised to use the 'spell-check' and 'grammar-check' functions of your word processor. LaTeX You are recommended to use the Elsevier article class elsarticle.cls (http://www.ctan.org/tex-archive/macros/latex/contrib/elsarticle) to prepare your manuscript and BibTeX (http://www.bibtex.org) to generate your bibliography. For detailed submission instructions, templates and other information on LaTeX, see https://www.elsevier.com/latex.
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Article structure Subdivision - numbered sections Divide your article into clearly defined and numbered sections. Subsections should be numbered 1.1 (then 1.1.1, 1.1.2, ...), 1.2, etc. (the abstract is not included in section numbering). Use this numbering also for internal cross-referencing: do not just refer to 'the text'. Any subsection may be given a brief heading. Each heading should appear on its own separate line. Introduction State the objectives of the work and provide an adequate background, avoiding a detailed literature survey or a summary of the results. Materials and Methods Provide sufficient detail to allow the work to be reproduced. In the case of experimental papers the numerical purity (mass fraction or mole fraction) of the investigated substances should be indicated, as well as the method of purity determination, if known. Any subsequent purification of the sample, such as distillation, crystallization, drying, etc., should be described. Methods already published should be indicated by a reference: only relevant modifications should be described. Theory/calculation A Theory section should extend, not repeat, the background to the article already dealt with in the Introduction and lay the foundation for further work. In contrast, a Calculation section represents a practical development from a theoretical basis. Results Results should be clear and concise. Discussion This should explore the significance of the results of the work, not repeat them. A combined Results and Discussion section is often appropriate. Avoid extensive citations and discussion of published literature. Conclusions The main conclusions of the study may be presented in a short Conclusions section, which may stand alone or form a subsection of a Discussion or Results and Discussion section. Appendices If there is more than one appendix, they should be identified as A, B, etc. Formulae and equations in appendices should be given separate numbering: Eq. (A.1), Eq. (A.2), etc.; in a subsequent appendix, Eq. (B.1) and so on. Similarly for tables and figures: Table A.1; Fig. A.1, etc. Nomenclature Authors must provide a Nomenclature, to be published between the text of the paper and the list of references. The Nomenclature should be a list of all mathematical symbols in one column and their definitions with units, preferably including the equation number of first use, in an adjacent column. The symbols should follow the notation of the IUPAC, “Quantities, Units, and Symbols in Physical Chemistry, 2nd Ed.”, http://old.iupac.org/publications/books/gbook/green_book_2ed.pdf. In addition, all unusual abbreviations and acronyms used in the paper should be included in the Nomenclature. Authors should also consider defining symbols and acronyms when first used within the paper. Essential title page information • Title. Concise and informative. Titles are often used in information-retrieval systems. Avoid abbreviations and formulae where possible. • Author names and affiliations. Please clearly indicate the given name(s) and family name(s) of each author and check that all names are accurately spelled. Present the
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authors' affiliation addresses (where the actual work was done) below the names. Indicate all affiliations with a lower-case superscript letter immediately after the author's name and in front of the appropriate address. Provide the full postal address of each affiliation, including the country name and, if available, the e-mail address of each author. • Corresponding author. Clearly indicate who will handle correspondence at all stages of refereeing and publication, also post-publication. Ensure that the e-mail address is given and that contact details are kept up to date by the corresponding author. • Present/permanent address. If an author has moved since the work described in the
article was done, or was visiting at the time, a 'Present address' (or 'Permanent address') may
be indicated as a footnote to that author's name. The address at which the author actually did
the work must be retained as the main, affiliation address. Superscript Arabic numerals are
used for such footnotes. Abstract A concise and factual abstract is required. The abstract should state briefly the purpose of the research, the principal results and major conclusions. An abstract is often presented separately from the article, so it must be able to stand alone. For this reason, References should be avoided, but if essential, then cite the author(s) and year(s). Also, non-standard or uncommon abbreviations should be avoided, but if essential they must be defined at their first mention in the abstract itself. Graphical abstract Although a graphical abstract is optional, its use is encouraged as it draws more attention to the online article. The graphical abstract should summarize the contents of the article in a concise, pictorial form designed to capture the attention of a wide readership. Graphical abstracts should be submitted as a separate file in the online submission system. Image size: Please provide an image with a minimum of 531 × 1328 pixels (h × w) or proportionally more. The image should be readable at a size of 5 × 13 cm using a regular screen resolution of 96 dpi. Preferred file types: TIFF, EPS, PDF or MS Office files. See https://www.elsevier.com/graphicalabstracts for examples. Authors can make use of Elsevier's Illustration and Enhancement service to ensure the best presentation of their images and in accordance with all technical requirements: Illustration Service. Highlights Highlights are a short collection of bullet points that convey the core findings of the article. Highlights are optional and should be submitted in a separate file in the online submission system. Please include 3 to 5 bullet points (max. 85 characters per bullet point including spaces). See http://www.elsevier.com/researchhighlights for examples. Note: for Asian authors, interpreting a character as a word, max 85 characters per bullet point corresponds with approx. 20 words max per bullet point. Keywords Immediately after the abstract, provide a maximum of 5 keywords, using American spelling and avoiding general and plural terms and multiple concepts (avoid, for example, "and", "of"). Be sparing with abbreviations: only abbreviations firmly established in the field may be eligible. These keywords will be used for indexing purposes. Acknowledgements Collate acknowledgements in a separate section at the end of the article before the references and do not, therefore, include them on the title page, as a footnote to the title or otherwise. List here those individuals who provided help during the research (e.g., providing language help, writing assistance or proof reading the article, etc.).
Nomenclature and units Follow internationally accepted rules and conventions: use the international system of units (SI). If other quantities are mentioned, give their equivalent in SI. You are urged to consult IUPAC: Nomenclature of Inorganic Chemistry: http://www.iupac.org/ for further
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information. Math formulae Please submit math equations as editable text and not as images. Present simple formulae in line with normal text where possible and use the solidus (/) instead of a horizontal line for small fractional terms, e.g., X/Y. In principle, variables are to be presented in italics. Powers of e are often more conveniently denoted by exp. Number consecutively any equations that have to be displayed separately from the text (if referred to explicitly in the text). Footnotes Footnotes should be used sparingly. Number them consecutively throughout the article. Many word processors build footnotes into the text, and this feature may be used. Should this not be the case, indicate the position of footnotes in the text and present the footnotes themselves separately at the end of the article. Artwork Electronc artwork
General points • Make sure you use uniform lettering and sizing of your original artwork. • Preferred fonts: Arial (or Helvetica), Times New Roman (or Times), Symbol, Courier. • Number the illustrations according to their sequence in the text. • Use a logical naming convention for your artwork files. • Indicate per figure if it is a single, 1.5 or 2-column fitting image. • For Word submissions only, you may still provide figures and their captions, and tables within a single file at the revision stage. • Please note that individual figure files larger than 10 MB must be provided in separate source files. A detailed guide on electronic artwork is available on our website: https://www.elsevier.com/artworkinstructions. You are urged to visit this site; some excerpts from the detailed information are
given here. Formats Regardless of the application used, when your electronic artwork is finalized, please 'save as' or convert the images to one of the following formats (note the resolution requirements for line drawings, halftones, and line/halftone combinations given below): EPS (or PDF): Vector drawings. Embed the font or save the text as 'graphics'. TIFF (or JPG): Color or grayscale photographs (halftones): always use a minimum of 300 dpi. TIFF (or JPG): Bitmapped line drawings: use a minimum of 1000 dpi. TIFF (or JPG): Combinations bitmapped line/half-tone (color or grayscale): a minimum of 500 dpi is required. Please do not:
• Supply files that are optimized for screen use (e.g., GIF, BMP, PICT, WPG); the
resolution is too low. • Supply files that are too low in resolution. • Submit graphics that are disproportionately large for the content. Non-electronic artwork Provide all illustrations as high-quality printouts, suitable for reproduction (which may
include reduction) without retouching. Number illustrations consecutively in the order in
which they are referred to in the text. They should accompany the manuscript, but
should not be included within the text. Clearly mark all illustrations on the back (or - in
case of line drawings - on the lower front side) with the figure number and the author's
name and, in cases of ambiguity, the correct orientation.
Mark the appropriate position of a figure in the article. Figure captions Ensure that each illustration has a caption. A caption should comprise a brief title (not on the figure itself) and a description of the illustration. Keep text in the illustrations themselves to a minimum but explain all symbols and abbreviations used.
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Tables Please submit tables as editable text and not as images. Tables can be placed either next to the relevant text in the article, or on separate page(s) at the end. Number tables consecutively in accordance with their appearance in the text and place any table notes below the table body. Be sparing in the use of tables and ensure that the data presented in them do not duplicate results described elsewhere in the article. Please avoid using vertical rules. References Citation in text Please ensure that every reference cited in the text is also present in the reference list (and vice versa). Any references cited in the abstract must be given in full. Unpublished results and personal communications are not recommended in the reference list, but may be mentioned in the text. If these references are included in the reference list they should follow the standard reference style of the journal and should include a substitution of the publication date with either 'Unpublished results' or 'Personal communication'. Citation of a reference as 'in press' implies that the item has been accepted for publication. Reference links Increased discoverability of research and high quality peer review are ensured by online links to the sources cited. In order to allow us to create links to abstracting and indexing services, such as Scopus, CrossRef and PubMed, please ensure that data provided in the references are correct. Please note that incorrect surnames, journal/book titles, publication year and pagination may prevent link creation. When copying references, please be careful as they may already contain errors. Use of the DOI is encouraged. Web references As a minimum, the full URL should be given and the date when the reference was last accessed. Any further information, if known (DOI, author names, dates, reference to a source publication, etc.), should also be given. Web references can be listed separately (e.g., after the reference list) under a different heading if desired, or can be included in the reference list. References in a special issue Please ensure that the words 'this issue' are added to any references in the list (and any citations in the text) to other articles in the same Special Issue.
Reference management software
Most Elsevier journals have a standard template available in key reference management
packages. This covers packages using the Citation Style Language, such as Mendeley
(http://www.mendeley.com/features/reference-manager) and also others like EndNote
(http://www.endnote.com/support/enstyles.asp) and Reference Manager
(http://refman.com/support/rmstyles.asp). Using plug-ins to word processing packages
which are available from the above sites, authors only need to select the appropriate
journal template when preparing their article and the list of references and citations to
these will be formatted according to the journal style as described in this Guide. The
process of including templates in these packages is constantly ongoing. If the journal you
are looking for does not have a template available yet, please see the list of sample
references and citations provided in this Guide to help you format these according to the
journal style.
If you manage your research with Mendeley Desktop, you can easily install the reference
style for this journal by clicking the link below: http://open.mendeley.com/use-citation-
style/fluid-phase-equilibria When preparing your manuscript, you will then be able to
select this style using the Mendeley plugins for Microsoft Word or LibreOffice. For more
information about the Citation Style Language, visit http://citationstyles.org. Reference formatting There are no strict requirements on reference formatting at submission. References can
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be in any style or format as long as the style is consistent. Where applicable, author(s) name(s), journal title/book title, chapter title/article title, year of publication, volume number/book chapter and the pagination must be present. Use of DOI is highly encouraged. The reference style used by the journal will be applied to the accepted article by Elsevier at the proof stage. Note that missing data will be highlighted at proof stage for the author to correct. If you do wish to format the references yourself they should be arranged according to the following examples: Reference style Text: Indicate references by number(s) in square brackets in line with the text. The actual authors can be referred to, but the reference number(s) must always be given. Example: '....as demonstrated [3,6]. Barnaby and Jones [8] obtained a different result...' List: Number the references (numbers in square brackets) in the list in the order in which they appear in the text. Examples: Reference to a journal publication: [1] J. van der Geer, J.A.J. Hanraads, R.A. Lupton, The art of writing a scientific article, J. Sci. Commun. 163 (2010) 51–59. Reference to a book: [2] W. Strunk Jr., E.B. White, The Elements of Style, fourth ed., Longman, New York, 2000. Reference to a chapter in an edited book: [3] G.R. Mettam, L.B. Adams, How to prepare an electronic version of your article, in: B.S. Jones, R.Z. Smith (Eds.), Introduction to the Electronic Age, E-Publishing Inc., New York, 2009, pp. 281–304. Reference to a website: [4] Cancer Research UK, Cancer statistics reports for the UK. http://www.cancerresearchuk.org/ aboutcancer/statistics/cancerstatsreport/, 2003 (accessed 13.03.03). Journal Abbreviations Source Journal names should be abbreviated
according to Chemical Abstracts Service
(CAS): http://www.cas.org Video data Elsevier accepts video material and animation sequences to support and enhance your scientific research. Authors who have video or animation files that they wish to submit with their article are strongly encouraged to include links to these within the body of the article. This can be done in the same way as a figure or table by referring to the video or animation content and noting in the body text where it should be placed. All submitted files should be properly labeled so that they directly relate to the video file's content. In order to ensure that your video or animation material is directly usable, please provide the files in one of our recommended file formats with a preferred maximum size of 150 MB. Video and animation files supplied will be published online in the electronic version of your article in Elsevier Web products, including ScienceDirect: http://www.sciencedirect.com. Please supply 'stills' with your files: you can choose any frame from the video or animation or make a separate image. These will be used instead of standard icons and will personalize the link to your video data. For more detailed instructions please visit our video instruction pages at https://www.elsevier.com/artworkinstructions. Note: since video and animation cannot be embedded in the print version of the journal, please provide text for both the electronic and the print version for the portions of the article that refer to this content. AudioSlides The journal encourages authors to create an AudioSlides presentation with their published article. AudioSlides are brief, webinar-style presentations that are shown next to the online article on ScienceDirect. This gives authors the opportunity to summarize their research in their own words and to help readers understand what the paper is about. More information and examples are available at https://www.elsevier.com/audioslides. Authors of this journal will automatically receive an invitation e-mail to create an AudioSlides presentation after acceptance of their paper.
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Supplementary material Supplementary material can support and enhance your scientific research. Supplementary files offer the author additional possibilities to publish supporting applications, high-resolution images, background datasets, sound clips and more. Please note that such items are published online exactly as they are submitted; there is no typesetting involved (supplementary data supplied as an Excel file or as a PowerPoint slide will appear as such online). Please submit the material together with the article and supply a concise and descriptive caption for each file. If you wish to make any changes to supplementary data during any stage of the process, then please make sure to provide an updated file, and do not annotate any corrections on a previous version. Please also make sure to switch off the 'Track Changes' option in any Microsoft Office files as these will appear in the published supplementary file(s). For more detailed instructions please visit our artwork instruction pages at https://www.elsevier.com/artworkinstructions.
Database linking Elsevier encourages authors to connect articles with external databases, giving readers access to relevant databases that help to build a better understanding of the described research. Please refer to relevant database identifiers using the following format in your article: Database: xxxx (e.g., TAIR: AT1G01020; CCDC: 734053; PDB: 1XFN). See https://www.elsevier.com/databaselinking for more information and a full list of supported databases. Interactive plots This journal enables you to show an Interactive Plot with your article by simply submitting a data file. For instructions please go to https://www.elsevier.com/interactiveplots. Submission checklist The following list will be useful during the final checking of an article prior to sending it to the journal for review. Please consult this Guide for Authors for further details of any item. Ensure that the following items are present: One author has been designated as the corresponding author with contact details: • E-mail address • Full postal address
All necessary files have been uploaded, and contain: • Keywords • All figure captions • All tables (including title, description, footnotes) Further considerations • Manuscript has been 'spell-checked' and 'grammar-checked' • All references mentioned in the Reference list are cited in the text, and vice versa • Permission has been obtained for use of copyrighted material from other sources (including the Internet) Printed version of figures (if applicable) in color or black-and-white • Indicate clearly whether or not color or black-and-white in print is required.
For any further information please visit our customer support site at http://support.elsevier.com. AFTER ACCEPTANCE Use of the Digital Object Identifier The Digital Object Identifier (DOI) may be used to cite and link to electronic documents. The DOI consists of a unique alpha-numeric character string which is assigned to a document by the publisher upon the initial electronic publication. The assigned DOI never changes. Therefore, it is an ideal medium for citing a document, particularly 'Articles in press' because they have not yet received their full bibliographic information. Example of a correctly given DOI (in URL format; here an article in the journal Physics Letters B): http://dx.doi.org/10.1016/j.physletb.2010.09.059
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When you use a DOI to create links to documents on the web, the DOIs are guaranteed never to change. Online proof correction Corresponding authors will receive an e-mail with a link to our online proofing system, allowing annotation and correction of proofs online. The environment is similar to MS Word: in addition to editing text, you can also comment on figures/tables and answer questions from the Copy Editor. Web-based proofing provides a faster and less error-prone process by allowing you to directly type your corrections, eliminating the potential introduction of errors. If preferred, you can still choose to annotate and upload your edits on the PDF version. All instructions for proofing will be given in the e-mail we send to authors, including alternative methods to the online version and PDF. We will do everything possible to get your article published quickly and accurately. Please use this proof only for checking the typesetting, editing, completeness and correctness of the text, tables and figures. Significant changes to the article as accepted for publication will only be considered at this stage with permission from the Editor. It is important to ensure that all corrections are sent back to us in one communication. Please check carefully before replying, as inclusion of any subsequent corrections cannot be guaranteed. Proofreading is solely your responsibility.
Offprints At the time the issue which includes your article is about to be printed, you will receive your offprint in an electronic form at, i.e. a PDF file, via e-mail. Not only should an electronic offprint mean ease of use to you, but more so it will significantly decrease delivery time, and therefore we would hope you receive a better service from us. Authors wishing to order additional paid reprints should indicate the number of reprints required when returning proofs. The corresponding author, at no cost, will be provided with a personalized link providing 50 days free access to the final published version of the article on ScienceDirect. This link can also be used for sharing via email and social networks. For an extra charge, paper offprints can be ordered via the offprint order form which is sent once the article is accepted for publication. Both corresponding and co-authors may order offprints at any time via Elsevier's WebShop (http://webshop.elsevier.com/myarticleservices/offprints). Authors requiring printed copies of multiple articles may use Elsevier WebShop's 'Create Your Own Book' service to collate multiple articles within a single cover (http://webshop.elsevier.com/myarticleservices/booklets). AUTHOR INQUIRIES You can track your submitted article at https://www.elsevier.com/track-submission. You can track your accepted article at https://www.elsevier.com/trackarticle. You are also welcome to contact Customer Support via http://support.elsevier.com
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